<i>JAG1</i> and <i>THBS2</i> Mutations in a Child Presenting With Incomplete Alagille Syndrome.

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.

Afiliação

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 em En | MEDLINE | ID: mdl-37600608