Defective roles of ATP7B missense mutations in cellular copper tolerance and copper excretion
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Cell Biology,Cellular and Molecular Neuroscience,Molecular Biology
Reference31 articles.
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2. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene;Bull;Nat. Genet.,1993
3. Copper transport and its alterations in Menkes and Wilson diseases;DiDonato;Biochim. Biophys. Acta,1997
4. Adenosine triphosphate-dependent copper transport in isolated rat liver plasma membranes;Dijkstra;J. Clin. Invest.,1995
5. Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?;Forbes;Am. J. Hum. Genet.,1998
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