Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Biochemistry
Reference44 articles.
1. Copper transport and its alterations in Menkes and Wilson diseases
2. The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
3. Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
4. Isolation of a partial candidate gene for Menkes disease by positional cloning
5. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
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