{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T04:11:03Z","timestamp":1789963863038,"version":"4.0.1"},"reference-count":68,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2008,1,1]],"date-time":"2008-01-01T00:00:00Z","timestamp":1199145600000},"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":["Bone"],"published-print":{"date-parts":[[2008,1]]},"DOI":"10.1016\/j.bone.2007.08.029","type":"journal-article","created":{"date-parts":[[2007,8,31]],"date-time":"2007-08-31T07:14:59Z","timestamp":1188544499000},"page":"19-29","source":"Crossref","is-referenced-by-count":230,"title":["Genetics, pathogenesis and complications of osteopetrosis"],"prefix":"10.1016","volume":"42","author":[{"given":"Andrea","family":"Del Fattore","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alfredo","family":"Cappariello","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anna","family":"Teti","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.bone.2007.08.029_bib1","series-title":"Connective tissue and its heritable disorders: medical, genetic, and molecular aspects","first-page":"753","article-title":"Osteopetrosis","author":"Whyte","year":"2002"},{"key":"10.1016\/j.bone.2007.08.029_bib2","first-page":"365","article-title":"R\u00f6ntgenbilder einer seltenen Knockenerkrankung","volume":"5","author":"Albers-Sch\u00f6nberg","year":"1904","journal-title":"Munch Med Wochenschr"},{"key":"10.1016\/j.bone.2007.08.029_bib3","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1615\/CritRevEukaryotGeneExpr.v15.i2.40","article-title":"Lessons from osteopetrotic mutations in animals: impact on our current understanding of osteoclast biology","volume":"15","author":"Van Wesenbeeck","year":"2005","journal-title":"Crit Rev Eukaryot Gene Expr"},{"key":"10.1016\/j.bone.2007.08.029_bib4","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1038\/sj.bmt.1704194","article-title":"Long-term outcome of haematopoietic stem cell transplantation in autosomal recessive osteopetrosis: an EBMT report","volume":"32","author":"Driessen","year":"2003","journal-title":"Bone Marrow Transplant"},{"key":"10.1016\/j.bone.2007.08.029_bib5","doi-asserted-by":"crossref","first-page":"2","DOI":"10.1097\/00003086-198201000-00001","article-title":"The classic: osteopetrosis cured by temporary parabiosis","volume":"162","author":"Walker","year":"1982","journal-title":"Clin Orthop Relat Res"},{"key":"10.1016\/j.bone.2007.08.029_bib6","doi-asserted-by":"crossref","first-page":"4","DOI":"10.1097\/00003086-199309000-00002","article-title":"Bone resorption restored in osteopetrotic mice by transplants of normal bone marrow and spleen cells","volume":"294","author":"Walker","year":"1993","journal-title":"Clin Orthop Relat Res"},{"key":"10.1016\/j.bone.2007.08.029_bib7","doi-asserted-by":"crossref","first-page":"896","DOI":"10.1016\/S0022-3476(05)82004-9","article-title":"Bone marrow transplantation for autosomal recessive osteopetrosis. A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation Group","volume":"125","author":"Gerritsen","year":"1994","journal-title":"J Pediatr"},{"key":"10.1016\/j.bone.2007.08.029_bib8","doi-asserted-by":"crossref","first-page":"638","DOI":"10.1038\/nrg1122","article-title":"Genetic regulation of osteoclast development and function","volume":"4","author":"Teitelbaum","year":"2003","journal-title":"Nat Rev Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib9","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1016\/j.exphem.2005.11.010","article-title":"Neonatal hematopoietic stem cell transplantation cures oc\/oc mice from osteopetrosis","volume":"34","author":"Johansson","year":"2006","journal-title":"Exp Hematol"},{"key":"10.1016\/j.bone.2007.08.029_bib10","doi-asserted-by":"crossref","first-page":"14629","DOI":"10.1073\/pnas.0507637102","article-title":"Rescue of ATPa3-deficient murine malignant osteopetrosis by hematopoietic stem cell transplantation in utero","volume":"102","author":"Frattini","year":"2005","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.bone.2007.08.029_bib11","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1016\/0221-8747(84)90027-4","article-title":"Congenitally osteopetrotic (op\/op) mice are not cured by transplants of spleen or bone marrow cells from normal littermates","volume":"5","author":"Marks","year":"1984","journal-title":"Metab Bone Dis Relat Res"},{"key":"10.1016\/j.bone.2007.08.029_bib12","doi-asserted-by":"crossref","first-page":"514","DOI":"10.1002\/jemt.10375","article-title":"Osteoclast diseases","volume":"61","author":"Helfrich","year":"2003","journal-title":"Microsc Res Tech"},{"key":"10.1016\/j.bone.2007.08.029_bib13","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1016\/S8756-3282(01)00656-1","article-title":"Macrophage colony-stimulating factor and receptor activator NF-kappaB ligand fail to rescue osteoclast-poor human malignant infantile osteopetrosis in vitro","volume":"30","author":"Flanagan","year":"2002","journal-title":"Bone"},{"key":"10.1016\/j.bone.2007.08.029_bib14","doi-asserted-by":"crossref","first-page":"198","DOI":"10.1016\/S0720-048X(01)00400-4","article-title":"Molecular and radiological diagnosis of sclerosing bone dysplasias","volume":"40","author":"Van Hul","year":"2001","journal-title":"Eur J Radiol"},{"key":"10.1016\/j.bone.2007.08.029_bib15","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1016\/S0092-8674(01)00206-9","article-title":"Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man","volume":"104","author":"Kornak","year":"2001","journal-title":"Cell"},{"key":"10.1016\/j.bone.2007.08.029_bib16","doi-asserted-by":"crossref","first-page":"1079","DOI":"10.1038\/sj.emboj.7600576","article-title":"Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration","volume":"24","author":"Kasper","year":"2005","journal-title":"EMBO J"},{"key":"10.1016\/j.bone.2007.08.029_bib17","doi-asserted-by":"crossref","first-page":"220","DOI":"10.1038\/nature04535","article-title":"ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function","volume":"440","author":"Lange","year":"2006","journal-title":"Nature"},{"key":"10.1016\/j.bone.2007.08.029_bib18","doi-asserted-by":"crossref","first-page":"263","DOI":"10.1007\/s00223-005-0027-6","article-title":"A clinical and molecular overview of the human osteopetroses","volume":"77","author":"Balemans","year":"2005","journal-title":"Calcif Tissue Int"},{"key":"10.1016\/j.bone.2007.08.029_bib19","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/8756-3282(88)90021-X","article-title":"Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis","volume":"9","author":"Bollerslev","year":"1988","journal-title":"Bone"},{"key":"10.1016\/j.bone.2007.08.029_bib20","doi-asserted-by":"crossref","first-page":"763","DOI":"10.1086\/368277","article-title":"Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density","volume":"72","author":"Van Wesenbeeck","year":"2003","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib21","doi-asserted-by":"crossref","first-page":"2371","DOI":"10.1093\/hmg\/11.20.2371","article-title":"The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes","volume":"11","author":"Smahi","year":"2002","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib22","doi-asserted-by":"crossref","first-page":"254","DOI":"10.1007\/s00277-002-0571-3","article-title":"Osteopetrosis and Glanzmann\u2019s thrombasthenia in a child","volume":"82","author":"Yarali","year":"2003","journal-title":"Ann Hematol"},{"key":"10.1016\/j.bone.2007.08.029_bib23","doi-asserted-by":"crossref","first-page":"664","DOI":"10.1097\/01.jnen.0000225905.52002.3e","article-title":"Carbonic anhydrase II in the developing and adult human brain","volume":"65","author":"Kida","year":"2006","journal-title":"J Neuropathol Exp Neurol"},{"key":"10.1016\/j.bone.2007.08.029_bib24","doi-asserted-by":"crossref","first-page":"252","DOI":"10.1016\/S0022-3476(05)80495-0","article-title":"Transient infantile osteopetrosis","volume":"118","author":"Monaghan","year":"1991","journal-title":"J Pediatr"},{"key":"10.1016\/j.bone.2007.08.029_bib25","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1002\/ajmg.1320280120","article-title":"Syndrome of osteopetrosis and muscular degeneration associated with cerebro-oculo-facio-skeletal changes","volume":"28","author":"Lerman-Seige","year":"1987","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib26","first-page":"528","article-title":"Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum","volume":"67","author":"Ben Hamouda","year":"2001","journal-title":"Acta Orthop Belg"},{"key":"10.1016\/j.bone.2007.08.029_bib27","doi-asserted-by":"crossref","first-page":"834","DOI":"10.1359\/jbmr.1999.14.5.834","article-title":"Association of intermediate osteopetrosis with poikiloderma","volume":"14","author":"Migliaccio","year":"1999","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib28","doi-asserted-by":"crossref","first-page":"218","DOI":"10.1097\/00001665-200403000-00007","article-title":"Surgical correction of craniosynostosis in malignant osteopetrosis","volume":"15","author":"Krimmel","year":"2004","journal-title":"J Craniofac Surg"},{"issue":"A50","key":"10.1016\/j.bone.2007.08.029_bib29","first-page":"e71","article-title":"Carbonic anhydrase type II deficiency","volume":"46","author":"Bolt","year":"2005","journal-title":"Am J Kidney Dis"},{"key":"10.1016\/j.bone.2007.08.029_bib30","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1038\/77131","article-title":"Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis","volume":"25","author":"Frattini","year":"2000","journal-title":"Nat Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib31","doi-asserted-by":"crossref","first-page":"2059","DOI":"10.1093\/hmg\/9.13.2059","article-title":"Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis","volume":"9","author":"Kornak","year":"2000","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib32","doi-asserted-by":"crossref","first-page":"2861","DOI":"10.1093\/hmg\/10.25.2861","article-title":"Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene","volume":"10","author":"Cleiren","year":"2001","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib33","doi-asserted-by":"crossref","first-page":"1740","DOI":"10.1359\/jbmr.2003.18.10.1740","article-title":"Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis","volume":"18","author":"Frattini","year":"2003","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib34","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1038\/nm842","article-title":"Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human","volume":"9","author":"Chalhoub","year":"2003","journal-title":"Nat Med"},{"key":"10.1016\/j.bone.2007.08.029_bib35","doi-asserted-by":"crossref","first-page":"919","DOI":"10.1172\/JCI30328","article-title":"PLEKHM1 is involved in osteoclastic vesicular transport and mutations in this gene cause osteopetrosis in incisors absent rat and human","volume":"117","author":"Van Wesenbeeck","year":"2007","journal-title":"J Clin Invest"},{"issue":"suppl1","key":"10.1016\/j.bone.2007.08.029_bib36","first-page":"CC002","article-title":"Focal osteosclerosis in an otherwise osteopenic female patient harbouring a new heterozygote mutation (R714C) of the osteopterosis gene, Pleckstrin Homolog Domain Conyaining Family M (with Run Domain) Member 1 (PLEKHM1)","volume":"80","author":"Del Fattore","year":"2007","journal-title":"Calcif. Tissue Int."},{"key":"10.1016\/j.bone.2007.08.029_bib37","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1136\/jmg.40.2.115","article-title":"A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis","volume":"40","author":"Bothwick","year":"2003","journal-title":"J Med Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib38","doi-asserted-by":"crossref","first-page":"1236","DOI":"10.1126\/science.273.5279.1236","article-title":"Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency","volume":"273","author":"Gelb","year":"1996","journal-title":"Science"},{"key":"10.1016\/j.bone.2007.08.029_bib39","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1136\/jmg.2005.036673","article-title":"Clinical, genetic, and cellular analysis of 49 osteopetrotic patients: implications for diagnosis and treatment","volume":"43","author":"Del Fattore","year":"2006","journal-title":"J Med Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib40","doi-asserted-by":"crossref","first-page":"960","DOI":"10.1038\/ng2076","article-title":"Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL","volume":"39","author":"Sobacchi","year":"2007","journal-title":"Nat Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib41","doi-asserted-by":"crossref","first-page":"1098","DOI":"10.1359\/jbmr.060403","article-title":"Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement","volume":"21","author":"Pangrazio","year":"2006","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib42","doi-asserted-by":"crossref","first-page":"427","DOI":"10.2353\/ajpath.2007.060834","article-title":"Osteoclasts: what do they do and how do they do it?","volume":"170","author":"Teitelbaum","year":"2007","journal-title":"Am J Pathol"},{"key":"10.1016\/j.bone.2007.08.029_bib43","doi-asserted-by":"crossref","first-page":"533","DOI":"10.1080\/03605310600912709","article-title":"Calculating risk\/benefit in X-linked severe combined immune deficiency disorder (X-SCID) gene therapy trials: the task of ethical evaluation","volume":"31","author":"Swazo","year":"2006","journal-title":"J Med Philos"},{"key":"10.1016\/j.bone.2007.08.029_bib44","doi-asserted-by":"crossref","first-page":"1513","DOI":"10.1359\/jbmr.2003.18.8.1513","article-title":"Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II","volume":"18","author":"Waguespack","year":"2003","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib45","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1016\/S8756-3282(99)00244-6","article-title":"Type II autosomal dominant osteopetrosis (Albers-Schonberg disease): clinical and radiological manifestations in 42 patients","volume":"26","author":"Benichou","year":"2000","journal-title":"Bone"},{"key":"10.1016\/j.bone.2007.08.029_bib46","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1016\/0014-5793(95)01298-2","article-title":"ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family","volume":"377","author":"Brandt","year":"1995","journal-title":"FEBS Lett."},{"key":"10.1016\/j.bone.2007.08.029_bib47","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1002\/ajmg.a.30490","article-title":"Intrafamilial phenotypic variability of osteopetrosis due to chloride channel 7 (CLCN7) mutations","volume":"133","author":"Campos-Xavier","year":"2005","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.bone.2007.08.029_bib48","doi-asserted-by":"crossref","first-page":"771","DOI":"10.1210\/jc.2006-1986","article-title":"Autosomal dominant osteopetrosis: clinical severity and natural history of 94 subjects with a chloride channel 7 gene mutation","volume":"92","author":"Waguespack","year":"2007","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.bone.2007.08.029_bib49","doi-asserted-by":"crossref","first-page":"995","DOI":"10.1210\/jc.2005-2017","article-title":"Polymorphisms in the CLCN7 gene modulate bone density in postmenopausal women and in patients with autosomal dominant osteopetrosis type II","volume":"91","author":"Kornak","year":"2006","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.bone.2007.08.029_bib50","doi-asserted-by":"crossref","first-page":"655","DOI":"10.1016\/j.bone.2005.06.003","article-title":"Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes","volume":"37","author":"Chu","year":"2005","journal-title":"Bone"},{"key":"10.1016\/j.bone.2007.08.029_bib51","doi-asserted-by":"crossref","first-page":"1960","DOI":"10.1359\/JBMR.050717","article-title":"Polymorphisms of the CLCN7 gene are associated with BMD in women","volume":"20","author":"Pettersson","year":"2005","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib52","doi-asserted-by":"crossref","first-page":"1089","DOI":"10.1359\/jbmr.060409","article-title":"Disease status in autosomal dominant osteopetrosis type 2 is determined by osteoclastic properties","volume":"21","author":"Chu","year":"2006","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib53","doi-asserted-by":"crossref","first-page":"1329","DOI":"10.1359\/JBMR.040403","article-title":"In vitro differentiation of CD14 cells from osteopetrotic subjects: contrasting phenotypes with TCIRG1, CLCN7, and attachment defects","volume":"19","author":"Blair","year":"2004","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib54","doi-asserted-by":"crossref","first-page":"1537","DOI":"10.1016\/S0002-9440(10)63712-1","article-title":"Characterization of osteoclasts from patients harboring a G215R mutation in ClC-7 causing autosomal dominant osteopetrosis type II","volume":"164","author":"Henriksen","year":"2004","journal-title":"Am J Pathol"},{"key":"10.1016\/j.bone.2007.08.029_bib55","doi-asserted-by":"crossref","first-page":"2107","DOI":"10.1359\/jbmr.1999.14.12.2107","article-title":"Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structures","volume":"14","author":"Teti","year":"1999","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib56","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1359\/jbmr.070109","article-title":"Are nonresorbing osteoclasts sources of bone anabolic activity?","volume":"22","author":"Karsdal","year":"2007","journal-title":"J Bone Miner Res"},{"key":"10.1016\/j.bone.2007.08.029_bib57","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1016\/j.cmet.2006.05.012","article-title":"Bidirectional ephrinB2-EphB4 signaling controls bone homeostasis","volume":"4","author":"Zhao","year":"2006","journal-title":"Cell Metab"},{"key":"10.1016\/j.bone.2007.08.029_bib58","doi-asserted-by":"crossref","first-page":"5840","DOI":"10.1038\/sj.emboj.7601430","article-title":"Sphingosine 1-phosphate as a regulator of osteoclast differentiation and osteoclast\u2013osteoblast coupling","volume":"25","author":"Ryu","year":"2006","journal-title":"EMBO J"},{"key":"10.1016\/j.bone.2007.08.029_bib59","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1016\/j.molmed.2004.12.004","article-title":"Osteoclast-derived activity in the coupling of bone formation to resorption","volume":"11","author":"Martin","year":"2005","journal-title":"Trends Mol Med"},{"key":"10.1016\/j.bone.2007.08.029_bib60","doi-asserted-by":"crossref","first-page":"159","DOI":"10.1016\/8756-3282(89)90048-3","article-title":"Biomechanical competence of iliac crest trabecular bone in autosomal dominant osteopetrosis type I","volume":"10","author":"Bollerslev","year":"1989","journal-title":"Bone"},{"key":"10.1016\/j.bone.2007.08.029_bib61","doi-asserted-by":"crossref","first-page":"883","DOI":"10.1373\/clinchem.2003.029355","article-title":"Osteoclast-derived serum tartrate-resistant acid phosphatase 5b in Albers-Schonberg disease (type II autosomal dominant osteopetrosis)","volume":"50","author":"Alatalo","year":"2004","journal-title":"Clin Chem"},{"key":"10.1016\/j.bone.2007.08.029_bib62","doi-asserted-by":"crossref","first-page":"467","DOI":"10.1016\/S0002-9440(10)62269-9","article-title":"Acidification of the osteoclastic resorption compartment provides insight into the coupling of bone formation to bone resorption","volume":"166","author":"Karsdal","year":"2005","journal-title":"Am J Pathol"},{"key":"10.1016\/j.bone.2007.08.029_bib63","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1016\/S0002-9440(10)63798-4","article-title":"Genotype\u2013phenotype relationship in human ATP6i-dependent autosomal recessive osteopetrosis","volume":"162","author":"Taranta","year":"2003","journal-title":"Am J Pathol"},{"key":"10.1016\/j.bone.2007.08.029_bib64","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1210\/endo-126-2-955","article-title":"Osteopetrosis in the rat: coexistence of reductions in osteocalcin and bone resorption","volume":"126","author":"Lian","year":"1990","journal-title":"Endocrinology"},{"key":"10.1016\/j.bone.2007.08.029_bib65","doi-asserted-by":"crossref","first-page":"1835","DOI":"10.1172\/JCI118984","article-title":"Demonstration of an osteoblast defect in two cases of human malignant osteopetrosis","volume":"98","author":"Lajeunesse","year":"1996","journal-title":"J Clin Invest"},{"key":"10.1016\/j.bone.2007.08.029_bib66","first-page":"19","article-title":"Osteoclasts control osteoblast activity","volume":"vol. 4","author":"Karsdal","year":"2007"},{"key":"10.1016\/j.bone.2007.08.029_bib67","doi-asserted-by":"crossref","first-page":"1403","DOI":"10.1038\/nm1514","article-title":"v-ATPase V0 subunit d2-deficient mice exhibit impaired osteoclast fusion and increased bone formation","volume":"12","author":"Lee","year":"2006","journal-title":"Nat Med"},{"key":"10.1016\/j.bone.2007.08.029_bib68","first-page":"1256","article-title":"Loss of anion exchanger 2 (Ae2) in mice results in osteopetrosis","volume":"21","author":"Jansen","year":"2006","journal-title":"J Bone Miner Res"}],"container-title":["Bone"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S8756328207006278?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S8756328207006278?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2023,5,13]],"date-time":"2023-05-13T19:47:45Z","timestamp":1684007265000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S8756328207006278"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,1]]},"references-count":68,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2008,1]]}},"alternative-id":["S8756328207006278"],"URL":"https:\/\/doi.org\/10.1016\/j.bone.2007.08.029","relation":{},"ISSN":["8756-3282"],"issn-type":[{"value":"8756-3282","type":"print"}],"subject":[],"published":{"date-parts":[[2008,1]]}}}