Heterozygous ABCB4 mutations in children with cholestatic liver disease-Reference-Cited by-同舟云学术

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Heterozygous ABCB4 mutations in children with cholestatic liver disease

Published:2015-08-03 Issue:2 Volume:36 Page:258-267
ISSN:1478-3223
Container-title:Liver International
language:en
Short-container-title:Liver Int

Author:

Gordo-Gilart Raquel¹,Hierro Loreto¹²,Andueza Sara¹,Muñoz-Bartolo Gema¹²,López Carola³,Díaz Carmen¹²,Jara Paloma¹²,Álvarez Luis¹

Affiliation:

1. La Paz University Hospital Health Research Institute-IdiPAZ; Madrid Spain

2. Pediatric Liver Service; La Paz Children's University Hospital; Madrid Spain

3. Pediatric Gastroenterology; Hepatology and Nutrition Unit; Pereira Rossell Hospital; Montevideo Uruguay

Funder

Instituto de Salud Carlos III-Fondos FEDER

Fundación ACS

Publisher

Wiley

Subject

Hepatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/liv.12910/fullpdf

Reference49 articles.

1. Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis;Deleuze;Hepatology,1996

2. Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis;Vree;Proc Natl Acad Sci USA,1998

3. The multiple facets of ABCB4 (MDR3) deficiency;Sundaram;Curr Treat Options Gastroenterol,2007

4. The spectrum of liver diseases related to ABCB4 gene mutations: pathophysiology and clinical aspects;Davit-Spraul;Semin Liver Dis,2010

5. Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease;Smit;Cell,1993

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