{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,30]],"date-time":"2026-06-30T07:40:24Z","timestamp":1782805224739,"version":"3.54.5"},"reference-count":20,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2004,7,1]],"date-time":"2004-07-01T00:00:00Z","timestamp":1088640000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2004,7,1]],"date-time":"2004-07-01T00:00:00Z","timestamp":1088640000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["ajkd.org","clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["American Journal of Kidney Diseases"],"published-print":{"date-parts":[[2004,7]]},"DOI":"10.1053\/j.ajkd.2004.03.033","type":"journal-article","created":{"date-parts":[[2005,12,13]],"date-time":"2005-12-13T11:49:20Z","timestamp":1134474560000},"page":"64-70","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":48,"title":["Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis"],"prefix":"10.1053","volume":"44","author":[{"given":"Suchai","family":"Sritippayawan","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Achra","family":"Sumboonnanonda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Somkiat","family":"Vasuvattakul","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thitima","family":"Keskanokwong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nunghathai","family":"Sawasdee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Atchara","family":"Paemanee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peti","family":"Thuwajit","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Prapon","family":"Wilairat","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sumalee","family":"Nimmannit","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Prida","family":"Malasit","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pa-thai","family":"Yenchitsomanus","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"suppl 5","key":"10.1053\/j.ajkd.2004.03.033_BIB1","first-page":"S41","article-title":"The AE gene family of Cl\u2212\/HCO3\u2212 exchangers","volume":"15","author":"Alper","year":"2002","journal-title":"J Nephrol"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB2","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1038\/316234a0","article-title":"Primary structure and transmembrane orientation of the murine anion exchange protein","volume":"316","author":"Kopito","year":"1985","journal-title":"Nature"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB3","first-page":"F506","article-title":"Colocalization of H(+)-ATPase and band 3 anion exchanger in rabbit collecting duct intercalated cells","volume":"260","author":"Schuster","year":"1991","journal-title":"Am J Physiol"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB4","first-page":"F813","article-title":"Anion exchanger 1 in human kidney and oncocytoma differs from erythroid AE1 in its NH2 terminus","volume":"265","author":"Kollert-Jons","year":"1993","journal-title":"Am J Physiol"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB5","doi-asserted-by":"crossref","first-page":"1693","DOI":"10.1172\/JCI119694","article-title":"Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene","volume":"100","author":"Bruce","year":"1997","journal-title":"J Clin Invest"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB6","doi-asserted-by":"crossref","first-page":"6380","DOI":"10.1074\/jbc.273.11.6380","article-title":"Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl\u2212\/HCO3\u2212 exchanger","volume":"273","author":"Jarolim","year":"1998","journal-title":"J Biol Chem"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB7","doi-asserted-by":"crossref","first-page":"6337","DOI":"10.1073\/pnas.95.11.6337","article-title":"Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis","volume":"95","author":"Karet","year":"1998","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB8","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1007\/s004670000454","article-title":"Atypical distal renal tubular acidosis confirmed by mutation analysis","volume":"15","author":"Weber","year":"2000","journal-title":"Pediatr Nephrol"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB9","doi-asserted-by":"crossref","first-page":"644","DOI":"10.1007\/s00467-003-1112-6","article-title":"A de novo R589C mutation of anion exchanger 1 causing distal renal tubular acidosis","volume":"18","author":"Sritippayawan","year":"2003","journal-title":"Pediatr Nephrol"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB10","doi-asserted-by":"crossref","first-page":"2173","DOI":"10.1172\/JCI4836","article-title":"Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A","volume":"102","author":"Tanphaichitr","year":"1998","journal-title":"J Clin Invest"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB11","doi-asserted-by":"crossref","first-page":"1674","DOI":"10.1046\/j.1523-1755.1999.00756.x","article-title":"Autosomal recessive distal renal tubular acidosis associated with Southeast Asian ovalocytosis","volume":"56","author":"Vasuvattakul","year":"1999","journal-title":"Kidney Int"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB12","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1042\/bj3500041","article-title":"Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea","volume":"350","author":"Bruce","year":"2000","journal-title":"Biochem J"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB13","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1053\/ajkd.2002.33909","article-title":"Autosomal recessive distal renal tubular acidosis caused by G701D mutation of anion exchanger 1 gene","volume":"40","author":"Yenchitsomanus","year":"2002","journal-title":"Am J Kidney Dis"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB14","first-page":"651","article-title":"Human anion exchanger1 mutations and distal renal tubular acidosis","volume":"34","author":"Yenchitsomanus","year":"2003","journal-title":"Southeast Asian J Trop Med Public Health"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB15","first-page":"1602","article-title":"Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3","volume":"96","author":"Ribeiro","year":"2000","journal-title":"Blood"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB16","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1046\/j.1523-1755.2002.00417.x","article-title":"Band 3 mutations, distal renal tubular acidosis, and Southeast Asian ovalocytosis","volume":"62","author":"Wrong","year":"2002","journal-title":"Kidney Int"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB17","first-page":"259","article-title":"The excretion of acid in renal disease","volume":"28","author":"Wrong","year":"1959","journal-title":"Q J Med"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB18","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1007\/s10038-003-0059-6","article-title":"Anion exchanger 1 mutations associated with distal renal tubular acidosis in the Thai population","volume":"48","author":"Yenchitsomanus","year":"2003","journal-title":"J Hum Genet"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB19","doi-asserted-by":"crossref","first-page":"542","DOI":"10.1042\/bst0200542","article-title":"The defective red cell anion transporter (band 3) in hereditary South East Asian ovalocytosis and the role of glycophorin A in the expression of band 3 anion transport activity in Xenopus oocytes","volume":"20","author":"Tanner","year":"1992","journal-title":"Biochem Soc Trans"},{"key":"10.1053\/j.ajkd.2004.03.033_BIB20","doi-asserted-by":"crossref","first-page":"836","DOI":"10.1038\/355836a0","article-title":"Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells","volume":"355","author":"Schofield","year":"1992","journal-title":"Nature"}],"container-title":["American Journal of Kidney Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0272638604005165?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0272638604005165?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,3]],"date-time":"2025-10-03T01:28:48Z","timestamp":1759454928000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0272638604005165"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,7]]},"references-count":20,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2004,7]]}},"alternative-id":["S0272638604005165"],"URL":"https:\/\/doi.org\/10.1053\/j.ajkd.2004.03.033","relation":{},"ISSN":["0272-6386"],"issn-type":[{"value":"0272-6386","type":"print"}],"subject":[],"published":{"date-parts":[[2004,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis","name":"articletitle","label":"Article Title"},{"value":"American Journal of Kidney Diseases","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1053\/j.ajkd.2004.03.033","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2004 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}