Artigo Revisado por pares

CFC1 Gene Mutation and Biliary Atresia With Polysplenia Syndrome

2002; Lippincott Williams & Wilkins; Volume: 34; Issue: 3 Linguagem: Inglês

10.1002/j.1536-4801.2002.tb07616.x

ISSN

1536-4801

Autores

Emmanuel Jacquemin, Danièle Cresteil, Nicole Raynaud, Michelle Hadchouel,

Tópico(s)

Intestinal Malrotation and Obstruction Disorders

Resumo

Journal of Pediatric Gastroenterology and NutritionVolume 34, Issue 3 p. 326-326 Letters to the Editor CFC1 Gene Mutation and Biliary Atresia With Polysplenia Syndrome Emmanuel Jacquemin, Emmanuel Jacquemin Hepatology Unit, Department of Pediatrics, Le Kremlin Bicêtre, France INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this authorDanièle Cresteil, Danièle Cresteil INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this authorNicole Raynaud, Nicole Raynaud INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this authorMichelle Hadchouel, Michelle Hadchouel Hepatology Unit, Department of Pediatrics, Le Kremlin Bicêtre, France INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this author Emmanuel Jacquemin, Emmanuel Jacquemin Hepatology Unit, Department of Pediatrics, Le Kremlin Bicêtre, France INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this authorDanièle Cresteil, Danièle Cresteil INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this authorNicole Raynaud, Nicole Raynaud INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this authorMichelle Hadchouel, Michelle Hadchouel Hepatology Unit, Department of Pediatrics, Le Kremlin Bicêtre, France INSERM, U 347 Bicêtre University Hospital, Le Kremlin Bicêtre, FranceSearch for more papers by this author First published: 01 March 2002 https://doi.org/10.1002/j.1536-4801.2002.tb07616.xCitations: 9Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1Bates MD, Bucuvalas JC, Alonso MH, et al. Biliary atresia: pathogenesis and treatment. Semin Liver Dis 1998; 18: 281–93. 10.1055/s-2007-1007164 CASPubMedWeb of Science®Google Scholar 2Carmi R, Magee CA, Neill CA, et al. Extrahepatic biliary atresia and associated anomalies: etiologic heterogeneity suggested by distinctive patterns of associations. Am J Med Genet 1993; 45: 683–93. 10.1002/ajmg.1320450606 CASPubMedWeb of Science®Google Scholar 3Bamford RN, Roessler E, Burdine RD, et al. Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects. Nat Genet 2000; 26: 365–9. 10.1038/81695 CASPubMedWeb of Science®Google Scholar Citing Literature Volume34, Issue3March 2002Pages 326-326 ReferencesRelatedInformation

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