Wilson Disease: High Prevalence in a Mountaineous Area of Crete
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/J.1469-1809.2005.00171.x/fullpdf
Reference25 articles.
1. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene;Bull;Nat Genet,1993
2. High prevalence of the H1069Q mutation in East German patients with Wilson disease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis;Caca;J Hepatol,2001
3. Spanish Group of FH. A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease;Castillo;Hum Mutat,2002
4. His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype;Duc;Eur J Hum Genet,1998
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