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JAG1 and THBS2 Mutations in a Child Presenting With Incomplete Alagille Syndrome.
Almes, Marion; Gardin, Antoine; Davit-Spraul, Anne; Bouligand, Jérôme; Habes, Dalila; Jacquemin, Emmanuel.
Affiliation
  • Almes M; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.
  • Gardin A; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France.
  • Davit-Spraul A; Pediatric Hepatology and Liver Transplantation Unit, National Reference Centre for Biliary Atresia and Genetic Cholestasis, FILFOIE, ERN RARE LIVER.
  • Bouligand J; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France.
  • Habes D; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, France.
  • Jacquemin E; Biochemistry Unit.
JPGN Rep ; 4(3): e338, 2023 Aug.
Article in En | MEDLINE | ID: mdl-37600608
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JPGN Rep Year: 2023 Document type: Article Country of publication: Estados Unidos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JPGN Rep Year: 2023 Document type: Article Country of publication: Estados Unidos