Functional Expression of the Wilson Disease Protein Reveals Mislocalization and Impaired Copper-Dependent Trafficking of the Common H1069Q Mutation

Autor:	Payne, Aimee S., Kelly, Edward J., Gitlin, Jonathan D.
Zdroj:	Proceedings of the National Academy of Sciences of the United States of America, 1998 Sep 01. 95(18), 10854-10859.
Databáze:	JSTOR Journals
Externí odkaz:	https://www.jstor.org/stable/45981 Zobrazit plný text záznamu