Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.

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 and Ferenci, Peter (2015) Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations. Journal of hepatology, 63 (1). pp. 156-63. ISSN 1600-0641

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Item Type:	Article
Divisions:	Ordensklinikum Linz Elisabethinen > Interne 4 - Gastroenterologie & Hepatologie, Stoffwechsel & Ernährungsmedizin, Endokrinologie
Depositing User:	Prof. Dr. Rainer Schöfl
Date Deposited:	29 Oct 2019 12:32
Last Modified:	17 Feb 2025 09:33
URI:	https://eprints.vinzenzgruppe.at/id/eprint/8765

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