HUEY-LING CHEN2020-03-102020-03-1020130815-9319https://www.scopus.com/inward/record.uri?eid=2-s2.0-84874383578&doi=10.1111%2fjgh.12114&partnerID=40&md5=288a2b3a6e30f2f3298fbf1e2bf73b8ahttps://scholars.lib.ntu.edu.tw/handle/123456789/475102English[SDGs]SDG3ABC transporter; ABCB11 protein; ABCB4 protein; ATP8B1 protein; biological marker; cardiolipin; familial intrahepatic cholestasis 1 protein; gamma glutamyltransferase; Jagged1; Notch2 receptor; unclassified drug; Alagille syndrome; bile duct disease; cholelithiasis; clinical feature; disease predisposition; DNA polymorphism; editorial; eye malformation; face malformation; gene mapping; gene mutation; genetic susceptibility; heart disease; homozygosity; human; idiopathic disease; intrahepatic cholestasis; phenotype; pneumonia; priority journal; progressive familial intrahepatic cholestasis; protein expression; vertebra malformationeditorial10.1111/jgh.121142-s2.0-84874383578