{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,28]],"date-time":"2026-08-28T15:59:35Z","timestamp":1787932775043,"version":"build-2784847793"},"reference-count":99,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[1999,12,1]],"date-time":"1999-12-01T00:00:00Z","timestamp":944006400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Best Practice &amp; Research Clinical Haematology"],"published-print":{"date-parts":[[1999,12]]},"DOI":"10.1053\/beha.1999.0049","type":"journal-article","created":{"date-parts":[[2002,7,28]],"date-time":"2002-07-28T21:49:59Z","timestamp":1027892999000},"page":"707-727","source":"Crossref","is-referenced-by-count":42,"title":["The hereditary stomatocytoses and allied disorders: congenital disorders of erythrocyte membrane permeability to Na and K"],"prefix":"10.1053","volume":"12","author":[{"given":"Gordon W","family":"Stewart","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.Jane H","family":"Turner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1053\/beha.1999.0049_RF1","series-title":"The Haemolytic Anaemias","volume":"1","author":"Dacie","year":"1985"},{"key":"10.1053\/beha.1999.0049_RF2","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1097\/00062752-199903000-00009","article-title":"Hereditary dehydrated and overhydrated stomatocytosis: recent advances","volume":"6","author":"Delaunay","year":"1999","journal-title":"Current Opinion in Haematology"},{"key":"10.1053\/beha.1999.0049_RF3","series-title":"Blood: Principles and Practice of Hematology","first-page":"1701","article-title":"Disorders of the red cell membrane","author":"Lux","year":"1995"},{"key":"10.1053\/beha.1999.0049_RF4","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1111\/j.1365-2141.1961.tb00341.x","article-title":"Stomatocytosis: a hereditary haemolytic anomaly associated with haemolytic anaemia","volume":"7","author":"Lock","year":"1961","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF5","doi-asserted-by":"crossref","first-page":"573","DOI":"10.1056\/NEJM196803142781101","article-title":"Congenital hemolytic anemia with high sodium, low potassium red cells. Studies of membrane permeability","volume":"278","author":"Zarkowsky","year":"1968","journal-title":"New England Journal of Medicine"},{"key":"10.1053\/beha.1999.0049_RF6","doi-asserted-by":"crossref","first-page":"376","DOI":"10.1111\/j.1600-0609.1987.tb00014.x","article-title":"Stomatocytosis, abnormal platelets and pseudo-homozygous hyperchesterolaemia","volume":"38","author":"Stewart","year":"1987","journal-title":"European Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF7","series-title":"Red Cell Membrane Antigens","first-page":"371","article-title":"The membrane defect in hereditary stomatocytosis","author":"Stewart","year":"1993"},{"key":"10.1053\/beha.1999.0049_RF8","series-title":"Cell Volume Regulation","first-page":"120","article-title":"Pathophysiology of abnormal cell volume in human red cells","author":"Ellory","year":"1998"},{"key":"10.1053\/beha.1999.0049_RF9","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1042\/cs0690309","article-title":"A family with mild xerocytosis showing increased cation permeability at low temperatures","volume":"69","author":"Stewart","year":"1985","journal-title":"Clinical Science"},{"key":"10.1053\/beha.1999.0049_RF10","doi-asserted-by":"crossref","first-page":"719","DOI":"10.1085\/jgp.88.6.719","article-title":"Volume-sensitive K transport in human erythrocytes","volume":"88","author":"Kaji","year":"1986","journal-title":"Journal of General Physiology"},{"key":"10.1053\/beha.1999.0049_RF11","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1016\/0005-2736(86)90338-X","article-title":"Evidence for the presence of volume-sensitive KCl transport in \u2018young\u2019 human red cells","volume":"858","author":"Hall","year":"1986","journal-title":"Biochima et Biophysica Acta"},{"key":"10.1053\/beha.1999.0049_RF12","doi-asserted-by":"crossref","first-page":"733","DOI":"10.1016\/S0006-3495(97)78106-2","article-title":"The monovalent cation \u2018leak\u2019 transport in human erythrocytes: an electroneutral exchange process","volume":"73","author":"Richter","year":"1997","journal-title":"Biophysical Journal"},{"key":"10.1053\/beha.1999.0049_RF13","doi-asserted-by":"crossref","first-page":"1055","DOI":"10.1046\/j.1365-2141.1999.01444.x","article-title":"Two British families with variants on the \u2018cryohydrocytosis\u2019 form of hereditary stomatocytosis","volume":"105","author":"Coles","year":"1999","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF14","doi-asserted-by":"crossref","first-page":"899","DOI":"10.1182\/blood.V61.5.899.899","article-title":"Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance","volume":"61","author":"Clark","year":"1983","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF15","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1177\/003591576706000108","article-title":"Stomatocytosis","volume":"60","author":"Meadow","year":"1967","journal-title":"Proceedings of the Royal Society of Medicine"},{"key":"10.1053\/beha.1999.0049_RF16","doi-asserted-by":"crossref","first-page":"1273","DOI":"10.1172\/JCI110726","article-title":"Missing band 7 membrane protein in two patients with high Na, low K erythrocytes","volume":"70","author":"Lande","year":"1982","journal-title":"Journal of Clinical Investigation"},{"key":"10.1053\/beha.1999.0049_RF17","doi-asserted-by":"crossref","first-page":"452","DOI":"10.1111\/j.1365-2141.1989.tb07731.x","article-title":"Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency","volume":"72","author":"Eber","year":"1989","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF18","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1016\/0167-4781(91)90047-P","article-title":"Cloning and nucleotide sequence of cDNA encoding human erythrocyte band 7 integral membrane protein","volume":"1090","author":"Hiebl-Dirschmied","year":"1991","journal-title":"Biochimica et Biophysica Acta"},{"key":"10.1053\/beha.1999.0049_RF19","doi-asserted-by":"crossref","first-page":"1593","DOI":"10.1182\/blood.V79.6.1593.1593","article-title":"Isolation of cDNA coding for a ubiquitous membrane protein deficient in high Na, low K stomatocytic erythrocytes","volume":"79","author":"Stewart","year":"1992","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF20","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1182\/blood.V38.2.184.184","article-title":"A new variant of hereditary hemolytic anemia with stomatocytosis and erythrocyte cation abnormality","volume":"38","author":"Miller","year":"1971","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF21","doi-asserted-by":"crossref","first-page":"1375","DOI":"10.1172\/JCI105829","article-title":"Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes","volume":"47","author":"Jaffe","year":"1968","journal-title":"Journal of Clinical Investigation"},{"key":"10.1053\/beha.1999.0049_RF22","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1002\/ajh.2830420107","article-title":"Hereditary hemolytic disease with increased red blood cell phosphatidylcholine and dehydration: one, two, or many disorders?","volume":"42","author":"Clark","year":"1993","journal-title":"American Journal of Hematology"},{"key":"10.1053\/beha.1999.0049_RF23","doi-asserted-by":"crossref","first-page":"810","DOI":"10.1086\/302024","article-title":"Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (q23-qter)","volume":"63","author":"Carella","year":"1998","journal-title":"American Journal of Human Genetics"},{"key":"10.1053\/beha.1999.0049_RF24","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1182\/blood.V38.4.445.445","article-title":"Hereditary hemolytic anemia associated with abnormal membrane lipids: mechanism of accumulation of phosphatidylcholine","volume":"38","author":"Shohet","year":"1971","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF25","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1002\/ajh.2830340306","article-title":"Excess of red cell membrane proteins in hereditary high-phosphatidylcholine hemolytic anemia","volume":"34","author":"Lane","year":"1990","journal-title":"American Journal of Hematology"},{"key":"10.1053\/beha.1999.0049_RF26","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1016\/0009-8981(81)90388-0","article-title":"Altered red blood cell surface area in hereditary xerocytosis","volume":"114","author":"Sauberman","year":"1981","journal-title":"Clinica Chimica Acta"},{"key":"10.1053\/beha.1999.0049_RF27","doi-asserted-by":"crossref","first-page":"631","DOI":"10.1172\/JCI110297","article-title":"Exercise-induced hemolysis in xerocytosis. Erythrocyte dehydration and shear sensitivity","volume":"68","author":"Platt","year":"1981","journal-title":"Journal of Clinical Investigation"},{"key":"10.1053\/beha.1999.0049_RF28","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1111\/j.1365-2141.1981.tb02735.x","article-title":"Red cell membrane response to hydrogen peroxide-sensitivity in hereditary xerocytosis and in other abnormal red cells","volume":"48","author":"Snyder","year":"1981","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF29","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1016\/0005-2736(89)90381-7","article-title":"Cation transport in oxidant-stressed human erythrocytes: heightened N-ethylmaleimide activation of passive K+ influx after mild peroxidation","volume":"983","author":"Sheerin","year":"1989","journal-title":"Biochimica et Biophysica Acta"},{"key":"10.1053\/beha.1999.0049_RF30","doi-asserted-by":"crossref","first-page":"906","DOI":"10.1542\/peds.35.6.906","article-title":"A new congenital hemolytic anaemia with deformed erythrocytes (?\u2018\u2018stomatocytes\u201d) and remarkable susceptibility of erythrocytes to cold hemolysis in vitro","volume":"35","author":"Miller","year":"1965","journal-title":"Pediatrics"},{"key":"10.1053\/beha.1999.0049_RF31","series-title":"Red Blood Cell and Lens Metabolism","first-page":"311","article-title":"Hemolytic anaemia resulting from abnormal red cell membrane cation permeability\u2014hydrocytosis and cryocytosis","author":"Mentzer","year":"1980"},{"key":"10.1053\/beha.1999.0049_RF32","series-title":"Membranes and Genetic Diseases","first-page":"137","article-title":"Membrane phospholipid organisation in pathologic human erythrocytes","author":"Lubin","year":"1982"},{"key":"10.1053\/beha.1999.0049_RF33","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1016\/S0140-6736(79)91437-5","article-title":"Familial pseudohyperkalaemia. A new syndrome","volume":"ii","author":"Stewart","year":"1979","journal-title":"Lancet"},{"key":"10.1053\/beha.1999.0049_RF34","doi-asserted-by":"crossref","first-page":"3120","DOI":"10.1182\/blood.V93.9.3120","article-title":"Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis)","volume":"93","author":"Iolascon","year":"1999","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF35","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1046\/j.1365-2141.1999.01191.x","article-title":"Hereditary stomatocytosis with marked pseudohyperkalaemia","volume":"104","author":"Coles","year":"1999","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF36","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1016\/0005-2736(85)90155-5","article-title":"Temperature sensitivity of potassium flux in red blood cells in the familial pseudohyperkalaemia syndrome","volume":"821","author":"Meenaghan","year":"1985","journal-title":"Biochimica et Biophysica Acta"},{"key":"10.1053\/beha.1999.0049_RF37","doi-asserted-by":"crossref","first-page":"909","DOI":"10.1056\/NEJM196904242801701","article-title":"Congenital haemolytic anaemia with high-sodium, low-potassium red cells. Studies of three generations of a family with a new variant","volume":"280","author":"Oski","year":"1969","journal-title":"New England Journal of Medicine"},{"key":"10.1053\/beha.1999.0049_RF38","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1016\/S0960-8966(99)00012-7","article-title":"Germline mosaicism of MPZ gene in Dejerine\u2013Sottas syndrome (HMSN III) associated with hereditary stomatocytosis","volume":"9","author":"Takashima","year":"1999","journal-title":"Neuromuscular Disorders"},{"key":"10.1053\/beha.1999.0049_RF39","doi-asserted-by":"crossref","first-page":"557","DOI":"10.1182\/blood.V44.4.557.557","article-title":"Hereditary stomatocytosis with hemolytic anemia in the dog","volume":"44","author":"Pinkerton","year":"1974","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF40","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1177\/030098589403100213","article-title":"Erythrocyte indices and volume distribution in a dog with stomatocytosis","volume":"31","author":"Brown","year":"1994","journal-title":"Veterinary Pathology"},{"key":"10.1053\/beha.1999.0049_RF41","doi-asserted-by":"crossref","first-page":"904","DOI":"10.1182\/blood.V84.3.904.904","article-title":"Normal cations and abnormal membrane lipids in the red blood cells of dogs with familial stomatocytosis-hypertrophic gastritis","volume":"84","author":"Slappendel","year":"1994","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF42","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1182\/blood.V46.3.337.337","article-title":"Characteristics of the membrane defect in the hereditary stomatocytosis syndrome","volume":"46","author":"Wiley","year":"1975","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF43","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1046\/j.1365-2141.1996.4881033.x","article-title":"Thrombo-embolic disease after splenectomy for hereditary stomatocytosis","volume":"93","author":"Stewart","year":"1996","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF44","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1111\/j.1365-2141.1966.tb00125.x","article-title":"Persistent post-splenectomy thrombocytosis and thrombo-embolism: a consequence of continuing anaemia","volume":"12","author":"Hirsh","year":"1966","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF45","doi-asserted-by":"crossref","first-page":"3451","DOI":"10.1182\/blood.V89.9.3451","article-title":"Abnormal erythrocyte endothelial adherence in hereditary stomatocytosis","volume":"89","author":"Smith","year":"1997","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF46","doi-asserted-by":"crossref","first-page":"629","DOI":"10.1183\/09031936.93.04050629","article-title":"Spherocytosis and pulmonary hypertension: coincidental occurrence or causal relationship?","volume":"4","author":"Verresen","year":"1991","journal-title":"European Respiratory Journal"},{"key":"10.1053\/beha.1999.0049_RF47","doi-asserted-by":"crossref","first-page":"5392","DOI":"10.1182\/blood.V87.12.5392.bloodjournal87125392","article-title":"Xerocytosis with concomitant intrauterine ascites: first description and therapeutic approach","volume":"90","author":"Entazami","year":"1996","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF48","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1046\/j.1365-2141.1998.00992.x","article-title":"A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema","volume":"103","author":"Grootenboer","year":"1998","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF49","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1111\/j.1365-2141.1979.tb03689.x","article-title":"Hereditary stomatocytosis: association of low 2,3-diphosphoglycerate with increased cation pumping by the red cell","volume":"41","author":"Wiley","year":"1979","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF50","doi-asserted-by":"crossref","first-page":"778","DOI":"10.1152\/jappl.1995.78.3.778","article-title":"Effect of RBC shape and deformability on pulmonary O2diffusing capacity and resistance to flow in rabbit lungs","volume":"78","author":"Betticher","year":"1995","journal-title":"Journal of Applied Physiology"},{"key":"10.1053\/beha.1999.0049_RF51","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1038\/286403a0","article-title":"Increased human red cell cation passive permeability below 12\u00b0C","volume":"286","author":"Stewart","year":"1980","journal-title":"Nature"},{"key":"10.1053\/beha.1999.0049_RF52","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1113\/jphysiol.1986.sp016124","article-title":"The dependence on external cation of sodium and potassium fluxes across the human red cell membrane at low temperatures","volume":"375","author":"Blackstock","year":"1986","journal-title":"Journal of Physiology"},{"key":"10.1053\/beha.1999.0049_RF53","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1113\/jphysiol.1970.sp009081","article-title":"Paradoxical temperature dependence of sodium and potassium fluxes in human red cells","volume":"207","author":"Wieth","year":"1970","journal-title":"Journal of Physiology"},{"key":"10.1053\/beha.1999.0049_RF54","series-title":"Foundations of Colloid Science","author":"Hunter","year":"1986"},{"key":"10.1053\/beha.1999.0049_RF55","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1021\/bi951692k","article-title":"Conformational order of phospholipids incorporated into human erythrocytes: an FTIR spectroscopy study","volume":"35","author":"Moore","year":"1996","journal-title":"Biochemistry"},{"key":"10.1053\/beha.1999.0049_RF56","doi-asserted-by":"crossref","first-page":"258","DOI":"10.1016\/S0005-2736(98)00231-4","article-title":"South-east Asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cells","volume":"1416","author":"Bruce","year":"1999","journal-title":"Biochimica et Biophysica Acta"},{"key":"10.1053\/beha.1999.0049_RF57","doi-asserted-by":"crossref","first-page":"817","DOI":"10.1111\/j.1365-2141.1995.tb05201.x","article-title":"Hereditary xerocytosis: a report of six unrelated Spanish families with leaky red cell syndrome and increased heat stability of the erythrocyte membrane","volume":"90","author":"Vives Corrons","year":"1995","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF58","first-page":"2134","article-title":"Dehydrated hereditary stomatocytosis is not linked to the hlK1 locus, a Gardos channel candidate, on chromosome 19q13.2","volume":"93","author":"Gallagher","year":"1999","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF59","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1002\/(SICI)1096-8652(199901)60:1<72::AID-AJH13>3.0.CO;2-8","article-title":"Exclusion of stomatin, alpha adducin and beta adducin loci in a large kindred with dehydrated hereditary stomatocytosis","volume":"60","author":"Innes","year":"1999","journal-title":"American Journal of Hematology"},{"key":"10.1053\/beha.1999.0049_RF60","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1159\/000133542","article-title":"The gene coding for erythrocyte membrane protein band 7.2b (EPB7.2) is located in band q34.1 of human chromosome 9","volume":"63","author":"Westberg","year":"1993","journal-title":"Cytogenetics and Cellular Genetics"},{"key":"10.1053\/beha.1999.0049_RF61","doi-asserted-by":"crossref","first-page":"2404","DOI":"10.1182\/blood.V93.7.2404","article-title":"Stomatocytosis is absent in \u2018\u2018stomatin\u201d-deficient murine red blood cells","volume":"93","author":"Zhu","year":"1999","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF62","doi-asserted-by":"crossref","first-page":"26358","DOI":"10.1074\/jbc.270.44.26358","article-title":"Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary stomatocytosis","volume":"270","author":"Gallagher","year":"1995","journal-title":"Journal of Biological Chemistry"},{"key":"10.1053\/beha.1999.0049_RF63","doi-asserted-by":"crossref","first-page":"521","DOI":"10.1006\/geno.1995.1273","article-title":"The organization of the gene (EPB72) encoding the human erythrocyte band 7 integral membrane protein (protein 7.2b)","volume":"30","author":"Unfried","year":"1995","journal-title":"Genomics"},{"key":"10.1053\/beha.1999.0049_RF64","doi-asserted-by":"crossref","first-page":"17221","DOI":"10.1074\/jbc.273.27.17221","article-title":"Oligomeric nature of the integral membrane protein stomatin","volume":"273","author":"Syners","year":"1998","journal-title":"Journal of Biological Chemistry"},{"key":"10.1053\/beha.1999.0049_RF65","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1016\/S0167-4781(97)00178-4","article-title":"Isolation, molecular characterization, and tissue-specific expression of a novel putative G protein-coupled receptor","volume":"1395","author":"Mayer","year":"1998","journal-title":"Biochimica et Biophysica Acta"},{"key":"10.1053\/beha.1999.0049_RF66","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1016\/S0014-5793(99)00417-2","article-title":"Cysteine 29 is the major palmitoylation site on stomatin","volume":"449","author":"Snyers","year":"1999","journal-title":"FEBS Letters"},{"key":"10.1053\/beha.1999.0049_RF67","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1006\/mcne.1999.0761","article-title":"Stomatin, a MEC-2 like protein, is expressed by mammalian sensory neurons","volume":"13","author":"Mannsfeldt","year":"1999","journal-title":"Molecular and Cellular Neuroscience"},{"key":"10.1053\/beha.1999.0049_RF68","doi-asserted-by":"crossref","first-page":"292","DOI":"10.1038\/378292a0","article-title":"A stomatin-like protein necessary for mechanosensation in C. elegans","volume":"378","author":"Huang","year":"1995","journal-title":"Nature"},{"key":"10.1053\/beha.1999.0049_RF69","doi-asserted-by":"crossref","first-page":"659","DOI":"10.1146\/annurev.physiol.59.1.659","article-title":"Molecular modeling of mechanotransduction in the nematode Caernorhabditis elegans","volume":"59","author":"Tavernarakis","year":"1997","journal-title":"Annual Review of Physiology"},{"key":"10.1053\/beha.1999.0049_RF70","doi-asserted-by":"crossref","first-page":"785","DOI":"10.1042\/bst0200785","article-title":"The integral band 7 membrane protein of the human erythrocyte membrane","volume":"20","author":"Stewart","year":"1992","journal-title":"Biochemical Society Transactions"},{"key":"10.1053\/beha.1999.0049_RF71","doi-asserted-by":"crossref","first-page":"463","DOI":"10.1038\/367463a0","article-title":"Amiloride-sensitive epithelial Na channel is made up of three homologous sub-units","volume":"367","author":"Canessa","year":"1994","journal-title":"Nature"},{"key":"10.1053\/beha.1999.0049_RF72","doi-asserted-by":"crossref","first-page":"5699","DOI":"10.1073\/pnas.92.12.5699","article-title":"A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system","volume":"92","author":"Schild","year":"1995","journal-title":"Proceedings of the National Academy of Sciences of the USA"},{"key":"10.1053\/beha.1999.0049_RF73","first-page":"685","article-title":"Syndrome de Liddle (ou pseudo-hyperaldost\u00e9ronisme). Evolution a long terme et \u00e9tude des fluxes potassiques \u00e9rythrocytaires dans 4 observations","volume":"49","author":"Noblins","year":"1992","journal-title":"Archives of French Paediatrics"},{"key":"10.1053\/beha.1999.0049_RF74","doi-asserted-by":"crossref","first-page":"2253","DOI":"10.1172\/JCI106722","article-title":"Abnormal membrane sodium transport in Liddle's syndrome","volume":"50","author":"Gardner","year":"1971","journal-title":"Journal of Clinical Investigation"},{"key":"10.1053\/beha.1999.0049_RF75","doi-asserted-by":"crossref","first-page":"425","DOI":"10.1016\/S0968-0004(99)01467-X","article-title":"The SPFH domain: a universal motif in membrane-associated proteins implicated in regulating targeted protein turnover","volume":"24","author":"Tavernarakis","year":"1999","journal-title":"Trends in Biochemical Sciences"},{"key":"10.1053\/beha.1999.0049_RF76","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1172\/JCI5713","article-title":"Defective regulation of the epithelial Na channel by Nedd4 in Liddle's syndrome","volume":"103","author":"Abriel","year":"1999","journal-title":"Journal of Clinical Investigation"},{"key":"10.1053\/beha.1999.0049_RF77","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1002\/jcp.1041470105","article-title":"Exosome formation during maturation of mammalian and avian reticulocytes: evidence that exosome release is a major route for externalization of obsolete membrane proteins","volume":"147","author":"Johnstone","year":"1991","journal-title":"Journal of Cellular Physiology"},{"key":"10.1053\/beha.1999.0049_RF78","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1006\/bbrc.1996.0992","article-title":"Human erythrocyte band 7.2b is preferentially labeled by a photoreactive phospholipid","volume":"224","author":"Desneves","year":"1996","journal-title":"Biochemical and Biophysical Research Communications"},{"key":"10.1053\/beha.1999.0049_RF79","doi-asserted-by":"crossref","first-page":"492","DOI":"10.1042\/bst025492s","article-title":"Trans-bilayer phospholipid movements in human red blood cells deficient in the 32kDa band 7.2b membrane protein, \u2018stomatin\u2019","volume":"25","author":"Ho","year":"1997","journal-title":"Biochemical Society Transactions"},{"key":"10.1053\/beha.1999.0049_RF80","doi-asserted-by":"crossref","first-page":"199","DOI":"10.3109\/09687689409160430","article-title":"Back and forth: the regulation and function of transbilayer phospholipid movement in eukaryotic cells","volume":"11","author":"Williamson","year":"1994","journal-title":"Molecular Membrane Biology"},{"key":"10.1053\/beha.1999.0049_RF81","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1111\/j.1365-2141.1990.tb07855.x","article-title":"Aplastic crisis caused by human parvovirus in two patients with hereditary stomatocytosis","volume":"76","author":"Mabin","year":"1990","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF82","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1002\/jss.400090212","article-title":"Membrane effects of imidoesters in hereditary stomatocytosis","volume":"9","author":"Mentzer","year":"1978","journal-title":"Journal of Supramolecular Structure and Cellular Biochemistry"},{"key":"10.1053\/beha.1999.0049_RF83","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1007\/BF01477477","article-title":"Role of the spleen in congenital stomatocytosis associated with high sodium low potassium erythrocytes","volume":"59","author":"Schroter","year":"1981","journal-title":"Klinische Wochenschrift"},{"key":"10.1053\/beha.1999.0049_RF84","series-title":"Membranes and Disease","first-page":"95","article-title":"Studies on the cation transport in high sodium and low potassium red cells in hereditary anemia associated with stomatocytosis","author":"Schroter","year":"1976"},{"key":"10.1053\/beha.1999.0049_RF85","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1182\/blood.V42.1.1.1","article-title":"Hereditary hemolytic anemia associated with abnormal membrane lipid. II. Ion permeability and transport abnormalities","volume":"42","author":"Shohet","year":"1973","journal-title":"Blood"},{"key":"10.1053\/beha.1999.0049_RF86","doi-asserted-by":"crossref","first-page":"159","DOI":"10.1203\/00006450-197104000-00003","article-title":"A new familial disorder with abnormal erythrocyte morphology and increased permeability of the erythrocytes to sodium and potassium","volume":"5","author":"Honig","year":"1971","journal-title":"Pediatric Research"},{"key":"10.1053\/beha.1999.0049_RF87","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1056\/NEJM197409052911003","article-title":"Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss","volume":"291","author":"Glader","year":"1974","journal-title":"New England Journal of Medicine"},{"key":"10.1053\/beha.1999.0049_RF88","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1002\/ajh.2830340104","article-title":"No beneficial effect of splenectomy in hereditary high red cell membrane phosphatidylcholine hemolytic anemia: clinical and membrane studies of 20 patients","volume":"34","author":"Otsuka","year":"1990","journal-title":"American Journal of Hematology"},{"key":"10.1053\/beha.1999.0049_RF89","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1111\/j.1365-2141.1992.tb04605.x","article-title":"Hereditary stomatocytosis: phenotypic expression of sodium transport and band 7 peptides in 44 cases","volume":"82","author":"Kanzaki","year":"1992","journal-title":"British Journal of Haematology"},{"key":"10.1053\/beha.1999.0049_RF90","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1016\/S0140-6736(80)91043-0","article-title":"Familial pseudohyperkalaemia","volume":"i","author":"Luciani","year":"1980","journal-title":"Lancet"},{"key":"10.1053\/beha.1999.0049_RF91","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1016\/S0140-6736(82)91724-X","article-title":"Possible screening test for familial pseudohyperkalaemia","volume":"ii","author":"Leadbetter","year":"1982","journal-title":"Lancet"},{"key":"10.1053\/beha.1999.0049_RF92","doi-asserted-by":"crossref","first-page":"557","DOI":"10.1042\/cs0730557","article-title":"Familial pseudohyperkalaemia: inhibition of erythrocyte K efflux at 4\u00b0C by quinine","volume":"73","author":"James","year":"1987","journal-title":"Clinical Science"},{"key":"10.1053\/beha.1999.0049_RF93","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1042\/cs0770213","article-title":"Altered erythrocyte cation permeability in familial pseudohyperkalaemia","volume":"77","author":"Dagher","year":"1989","journal-title":"Clinical Science"},{"key":"10.1053\/beha.1999.0049_RF94","first-page":"104","article-title":"Pseudo-hyperkaliemie. A propos d'une observation familiale","volume":"52","author":"Vantyghem","year":"1991","journal-title":"Annals of Endocrinology"},{"key":"10.1053\/beha.1999.0049_RF95","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1177\/000456329703400515","article-title":"Pseudohyperkalaemia, pseudohyponatraemia and pseudohypoglycaemia in a patient with hereditary stomatocytosis","volume":"34","author":"Kilpatrick","year":"1997","journal-title":"Annals of Clinical Biochemistry"},{"key":"10.1053\/beha.1999.0049_RF96","doi-asserted-by":"crossref","first-page":"749","DOI":"10.1136\/pgmj.70.828.749","article-title":"Pseudohyperkalaemia associated with hereditary spherocytosis in four members of a family","volume":"70","author":"Alani","year":"1994","journal-title":"Postgraduate Medical Journal"},{"key":"10.1053\/beha.1999.0049_RF97","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1080\/01652176.1991.9694282","article-title":"Familial stomatocytosis\u2013hypertrophic gastritis (FSHG), a newly recognised disease in the dog (Drentse patrijshond)","volume":"13","author":"Slappendel","year":"1991","journal-title":"Veterinary Quarterly"},{"key":"10.1053\/beha.1999.0049_RF98","doi-asserted-by":"crossref","first-page":"1156","DOI":"10.1046\/j.1365-2362.1996.530611.x","article-title":"Gastric mucosal phospholipids in dogs with familial stomatocytosis\u2013hypertrophic gastritis","volume":"26","author":"Renooij","year":"1996","journal-title":"European Journal of Clinical Investigation"},{"key":"10.1053\/beha.1999.0049_RF99","doi-asserted-by":"crossref","first-page":"115","DOI":"10.3109\/00313028409059086","article-title":"Inherited red cell dehydration: a hemolytic syndrome in search of a name","volume":"16","author":"Wiley","year":"1984","journal-title":"Pathology"}],"container-title":["Best Practice &amp; Research Clinical Haematology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S152169269990049X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S152169269990049X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2023,4,23]],"date-time":"2023-04-23T23:29:50Z","timestamp":1682292590000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S152169269990049X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1999,12]]},"references-count":99,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1999,12]]}},"alternative-id":["S152169269990049X"],"URL":"https:\/\/doi.org\/10.1053\/beha.1999.0049","relation":{},"ISSN":["1521-6926"],"issn-type":[{"value":"1521-6926","type":"print"}],"subject":[],"published":{"date-parts":[[1999,12]]}}}