Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype-Reference-Cited by-同舟云学术

Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype

Published:2014-08-25 Issue:1 Volume:61 Page:260-267
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Vaz Frédéric M.¹,Paulusma Coen C.²,Huidekoper Hidde³,de Ru Minke³,Lim Cynthia⁴,Koster Janet¹,Ho-Mok Kam²,Bootsma Albert H.¹,Groen Albert K.⁵,Schaap Frank G.²⁶,Oude Elferink Ronald P. J.²,Waterham Hans R.¹,Wanders Ronald J.A.¹

Affiliation:

1. Laboratory Genetic Metabolic Disease; Academic Medical Center; Amsterdam The Netherlands

2. Tytgat Institute for Liver and Intestinal Research; Academic Medical Center; Amsterdam The Netherlands

3. Department of Pediatrics; Academic Medical Center; Amsterdam The Netherlands

4. Department of Pediatrics; Waterlandziekenhuis; Purmerend The Netherlands

5. Department of Pediatrics; University of Groningen, University Medical Center Groningen; The Netherlands

6. Department of Surgery; NUTRIM School of Nutrition, Toxicology and Metabolism, Maastricht University; Maastricht The Netherlands

Publisher

Wiley

Subject

Hepatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/hep.27240/fullpdf

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3. Molecular cloning, chromosomal localization, and functional characterization of a human liver Na+/bile acid cotransporter;Hagenbuch;J Clin Invest,1994

4. Role of the intestinal bile acid transporters in bile acid and drug disposition;Dawson;Handb Exp Pharmacol,2011

5. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis;Bull;Nat Genet,1998

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