{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T09:08:50Z","timestamp":1790845730283,"version":"4.1.0"},"reference-count":19,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,5,1]],"date-time":"2017-05-01T00:00:00Z","timestamp":1493596800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","medical-hypotheses.com","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Medical Hypotheses"],"published-print":{"date-parts":[[2017,5]]},"DOI":"10.1016\/j.mehy.2017.03.015","type":"journal-article","created":{"date-parts":[[2017,3,9]],"date-time":"2017-03-09T10:05:21Z","timestamp":1489053921000},"page":"91-93","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":10,"special_numbering":"C","title":["Somatic mutation, a cause of biliary atresia: A hypothesis"],"prefix":"10.1016","volume":"102","author":[{"given":"Alexandre","family":"Fabre","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C\u00e9line","family":"Roman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bertrand","family":"Roquelaure","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.mehy.2017.03.015_b0005","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.jaut.2016.06.005","article-title":"Biliary atresia: a comprehensive review","volume":"73","author":"Lakshminarayanan","year":"2016","journal-title":"J Autoimmun"},{"key":"10.1016\/j.mehy.2017.03.015_b0010","doi-asserted-by":"publisher","first-page":"281","DOI":"10.1016\/j.clinre.2015.11.010","article-title":"Biliary atresia: clinical advances and perspectives","volume":"40","author":"Nizery","year":"2016","journal-title":"Clin Res Hepatol Gastroenterol"},{"key":"10.1016\/j.mehy.2017.03.015_b0015","doi-asserted-by":"publisher","first-page":"344","DOI":"10.1097\/MPG.0b013e318282a913","article-title":"International incidence and outcomes of biliary atresia","volume":"56","author":"Jimenez-Rivera","year":"2013","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"10.1016\/j.mehy.2017.03.015_b0020","doi-asserted-by":"publisher","first-page":"46","DOI":"10.1053\/j.gastro.2011.10.001","article-title":"Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review","volume":"142","author":"Molodecky","year":"2012","journal-title":"Gastroenterology"},{"issue":"8","key":"10.1016\/j.mehy.2017.03.015_b0025","doi-asserted-by":"publisher","first-page":"128","DOI":"10.1186\/1750-1172-8-128","article-title":"Aetiology of biliary atresia: What is actually known?","volume":"29","author":"Petersen","year":"2013","journal-title":"Orphanet J Rare Dis"},{"issue":"2","key":"10.1016\/j.mehy.2017.03.015_b0030","doi-asserted-by":"publisher","first-page":"200","DOI":"10.1016\/j.jpedsurg.2015.10.058","article-title":"Biliary atresia: from Australia to the zebrafish","volume":"51","author":"Davenport","year":"2016","journal-title":"J Pediatr Surg"},{"key":"10.1016\/j.mehy.2017.03.015_b0035","doi-asserted-by":"publisher","first-page":"e22","DOI":"10.1097\/MPG.0b013e31826a1044","article-title":"Discordant presentation of biliary atresia in premature monozygotic twins","volume":"57","author":"Fallon","year":"2013","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"10.1016\/j.mehy.2017.03.015_b0040","doi-asserted-by":"publisher","first-page":"205","DOI":"10.1017\/S1120962300025452","article-title":"Thalidomide-embryopathy in twins","volume":"19","author":"Jorgensen","year":"1970","journal-title":"Acta Genet Med Gemellol"},{"key":"10.1016\/j.mehy.2017.03.015_b0045","doi-asserted-by":"publisher","first-page":"695","DOI":"10.1097\/01.inf.0000078354.15385.76","article-title":"Congenital toxoplasmosis in twins: a report of fourteen consecutive cases and a comparison with published data","volume":"22","author":"Peyron","year":"2003","journal-title":"Pediatr Infect Dis J"},{"issue":"47","key":"10.1016\/j.mehy.2017.03.015_b0050","doi-asserted-by":"publisher","first-page":"857","DOI":"10.1002\/ajmg.1320470612","article-title":"Fetal alcohol syndrome in twins of alcoholic mothers: concordance of diagnosis and IQ","volume":"1993","author":"Streissguth","year":"1993","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.mehy.2017.03.015_b0055","doi-asserted-by":"publisher","first-page":"18","DOI":"10.1111\/j.1751-0813.1990.tb07385.x","article-title":"Congenital biliary atresia and jaundice in lambs and calves","volume":"67","author":"Harper","year":"1990","journal-title":"Aust Vet J"},{"issue":"341","key":"10.1016\/j.mehy.2017.03.015_b0060","doi-asserted-by":"publisher","first-page":"358","DOI":"10.1126\/science.1239503","article-title":"Genetics. Genome mosaicism\u2013one human, multiple genomes","volume":"26","author":"Lupski","year":"2013","journal-title":"Science"},{"key":"10.1016\/j.mehy.2017.03.015_b0065","doi-asserted-by":"publisher","first-page":"307","DOI":"10.1038\/nrg3424","article-title":"A genomic view of mosaicism and human disease","volume":"14","author":"Biesecker","year":"2013","journal-title":"Nat Rev Genet"},{"key":"10.1016\/j.mehy.2017.03.015_b0070","doi-asserted-by":"publisher","first-page":"1237758","DOI":"10.1126\/science.1237758","article-title":"Somatic mutation, genomic variation, and neurological disease","volume":"341","author":"Poduri","year":"2013","journal-title":"Science"},{"key":"10.1016\/j.mehy.2017.03.015_b0075","doi-asserted-by":"publisher","first-page":"395","DOI":"10.1038\/nm.3824","article-title":"Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy","volume":"21","author":"Lim","year":"2015","journal-title":"Nat Med"},{"key":"10.1016\/j.mehy.2017.03.015_b0080","doi-asserted-by":"publisher","first-page":"1954","DOI":"10.1038\/ajg.2014.346","article-title":"Somatic mosaicism in esophageal atresia","volume":"109","author":"Bednarczyk","year":"2014","journal-title":"Am J Gastroenterol"},{"issue":"3","key":"10.1016\/j.mehy.2017.03.015_b0085","doi-asserted-by":"publisher","first-page":"101","DOI":"10.1007\/s40142-015-0071-0","article-title":"Mosaicism in traditional mendelian diseases","volume":"2015","author":"Ting","year":"2015","journal-title":"Current Genet Med Rep"},{"key":"10.1016\/j.mehy.2017.03.015_b0090","doi-asserted-by":"publisher","first-page":"478","DOI":"10.1002\/ajmg.a.33851","article-title":"Variable expression of neurofibromatosis 1 in monozygotic twins","volume":"155A","author":"Rieley","year":"2011","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.mehy.2017.03.015_b0095","doi-asserted-by":"publisher","first-page":"E2134","DOI":"10.1002\/humu.21476","article-title":"Monozygotic twins discordant for neurofibromatosis type 1 due to a postzygotic NF1 gene mutation","volume":"32","author":"Vogt","year":"2011","journal-title":"Hum Mutat"}],"container-title":["Medical Hypotheses"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0306987717300543?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0306987717300543?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,9,3]],"date-time":"2018-09-03T18:00:34Z","timestamp":1535997634000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0306987717300543"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,5]]},"references-count":19,"alternative-id":["S0306987717300543"],"URL":"https:\/\/doi.org\/10.1016\/j.mehy.2017.03.015","relation":{},"ISSN":["0306-9877"],"issn-type":[{"value":"0306-9877","type":"print"}],"subject":[],"published":{"date-parts":[[2017,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Somatic mutation, a cause of biliary atresia: A hypothesis","name":"articletitle","label":"Article Title"},{"value":"Medical Hypotheses","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.mehy.2017.03.015","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}