Hepatic steatosis in Wilson disease – Role of copper and PNPLA3 mutations-Reference-Cited by-同舟云学术

Hepatic steatosis in Wilson disease – Role of copper and PNPLA3 mutations

Published:2015-07 Issue:1 Volume:63 Page:156-163
ISSN:0168-8278
Container-title:Journal of Hepatology
language:en
Short-container-title:Journal of Hepatology

Author:

Stättermayer Albert Friedrich,Traussnigg Stefan,Dienes Hans-Peter,Aigner Elmar,Stauber Rudolf,Lackner Karoline,Hofer Harald,Stift Judith,Wrba Friedrich,Stadlmayr Andreas,Datz Christian,Strasser Michael,Maieron Andreas,Trauner Michael,Ferenci Peter

Publisher

Elsevier BV

Subject

Hepatology

Reference53 articles.

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4. Wilson disease mutation database, from: .

5. Wilson disease: clinical presentation, treatment, and survival;Stremmel;Ann Intern Med,1991

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