Open AccessBiliary atresia combined Wilson disease identified by whole exome sequencing in Vietnamese patient with severe liver failure
Author(s) -
Nguyen Pham Anh Hoa,
Nguyễn Thị Kim Liên,
Nguyen Van Tung,
Ngọc-Lan Nguyen,
Nguyễn Thị Thanh Phương,
Nguyen Thi Mai Huong,
Hoang Ngoc Thach,
Huy-Hoang Nguyen
Publication year - 2022
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000028547
Subject(s) - medicine , exome sequencing , liver transplantation , progressive familial intrahepatic cholestasis , compound heterozygosity , intestinal atresia , liver disease , biliary atresia , jaundice , liver biopsy , sanger sequencing , gastroenterology , exome , pediatrics , mutation , transplantation , atresia , genetics , biopsy , gene , biology