COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2005.00524.x/fullpdf
Reference15 articles.
1. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene;Bull;Nat Genet,1993
2. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene;Tanzi;Nat Genet,1993
3. Role of copper in Indian childhood cirrhosis;Tanner;Am J Clin Nutr,1998
4. Endemic Tyrolean infantile cirrhosis: an ecogenetic disorder;Muller;Lancet,1996
5. Wilson disease and idiopathic copper toxicosis;Scheinberg;Am J Clin Nutr,1996
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