Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-010-9123-5
Reference46 articles.
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2. Ala A et al (2007) Wilson’s disease. Lancet 369(9559):397–408
3. Bull PC et al (1993) The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet 5(4):327–337
4. Burstein E et al (2004) A novel role for XIAP in copper homeostasis through regulation of MURR1. EMBO J 23(1):244–254
5. Coronado VA et al (2005) COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology. Clin Genet 68(6):548–551
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