Organic solute transporter-β (SLC51B) deficiency in two brothers with congenital diarrhea and features of cholestasis-Reference-Cited by-同舟云学术

Organic solute transporter-β (SLC51B) deficiency in two brothers with congenital diarrhea and features of cholestasis

Published:2018-05-11 Issue:2 Volume:68 Page:590-598
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Sultan Mutaz¹,Rao Anuradha²,Elpeleg Orly³,Vaz Frédéric M.⁴,Abu-Libdeh Bassam¹,Karpen Saul J.²,Dawson Paul A.²^ORCID

Affiliation:

1. Department of Pediatrics, Makassed Hospital; Al-Quds University, Faculty of Medicine; Jerusalem

2. Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition, Emory University School of Medicine; Children's Healthcare of Atlanta; Atlanta GA

3. Monique and Jacques Roboh Department of Genetic Research, Hadassah; Hebrew University Medical Center; Jerusalem Israel

4. Laboratory Genetic Metabolic Diseases; Academic Medical Center; Amsterdam Netherlands

Funder

National Institutes of Health

Publisher

Wiley

Subject

Hepatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/hep.29516/fullpdf

Reference19 articles.

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2. Primary bile acid malabsorption caused by mutations in the ileal sodium-dependent bile acid transporter gene (SLC10A2);Oelkers;J Clin Invest,1997

3. The farnesoid X receptor: good for BAD;Keely;Cell Mol Gastroenterol Hepatol,2016

4. Intestinal transport and metabolism of bile acids;Dawson;J Lipid Res,2015

5. Not all (bile acids) who wander are lost: the first report of a patient with an isolated NTCP defect;Karpen;Hepatology,2015

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