Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference44 articles.
1. The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
2. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
3. Isolation and Characterization of a Human Liver cDNA as a Candidate Gene for Wilson Disease
4. Biochemical Characterization of the Wilson Disease Protein and Functional Expression in the Yeast Saccharomyces cerevisiae
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