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JAG1 and THBS2 Mutations in a Child Presenting With Incomplete Alagille Syndrome.

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Title: JAG1 and THBS2 Mutations in a Child Presenting With Incomplete Alagille Syndrome.
Authors: Almes M; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France., Gardin A; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France., Davit-Spraul A; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France.; Biochemistry Unit., Bouligand J; Molecular Genetics and Pharmacogenetics, Bicêtre Hospital, Assistance Publique - Hôpitaux de Paris, University Paris-Saclay, Le Kremlin-Bicêtre, France., Habes D; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France., Jacquemin E; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France.
Source: JPGN reports [JPGN Rep] 2023 Jul 17; Vol. 4 (3), pp. e338. Date of Electronic Publication: 2023 Jul 17 (Print Publication: 2023).
Publication Type: Journal Article
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101773885 Publication Model: eCollection Cited Medium: Internet ISSN: 2691-171X (Electronic) Linking ISSN: 2691171X NLM ISO Abbreviation: JPGN Rep Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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      – TitleFull: JAG1 and THBS2 Mutations in a Child Presenting With Incomplete Alagille Syndrome.
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              Text: 2023 Jul 17
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