Open AccessHNF1B Mutation: A Rare Cause of Syndromic Biliary Hypoplasia and Neonatal Cholestasis
Author(s) -
Ashok Goyal
Publication year - 2021
Publication title -
tropical gastroenterology
Language(s) - English
Resource type - Journals
eISSN - 2320-5792
pISSN - 0250-636X
DOI - 10.7869/tg.655
Subject(s) - cholestasis , neonatal cholestasis , hypoplasia , medicine , mutation , progressive familial intrahepatic cholestasis , gastroenterology , pediatrics , genetics , biology , biliary atresia , liver transplantation , gene , transplantation