Maladie de Wilson : un cas et revue de la littérature
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry
Reference32 articles.
1. A clinical and biochemical study of hepatolenticular degeneration (Wilson's disease);Bickel;Q J Med,1957
2. Evidence for linkage between Wilson disease and esterase D in three kindreds : detection of linkage for an autosomal recessive disorder by the family study method;Bonne-Tamir;Genet Epidemiol,1986
3. Eight closely linked loci place the Wilson disease locus within 13q14-q21;Bowcock;Am J Hum Genet,1988
4. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene;Bull;Nature Genet,1993
5. Studies on copper metabolism. XVI. Radioactive copper studies in normal subjects and in patients with hepatolenticular degeneration;Bush;J Clin Invest,1955
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