Not all (bile acids) who wander are lost: The first report of a patient with an isolated NTCP defect
Author:
Affiliation:
1. Department of Pediatrics, Division of Pediatric Gastroenterology; Hepatology and Nutrition, Emory University School of Medicine, Children's Healthcare of Atlanta; Atlanta GA
Funder
National Institutes of Health
Publisher
Wiley
Subject
Hepatology
Reference21 articles.
1. Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: conjugated hypercholanemia without a clear clinical phenotype;Vaz;Hepatology,2015
2. Hepatocanalicular transport defects: pathophysiologic mechanisms of rare diseases;Oude Elferink;Gastroenterology,2006
3. Bile acid transporters;Dawson;J Lipid Res,2009
4. Ethnicity-dependent polymorphism in Na+-taurocholate cotransporting polypeptide (SLC10A1) reveals a domain critical for bile acid substrate recognition;Ho;J Biol Chem,2004
5. Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT;Carlton;Nat Genet,2003
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