High prevalence of the H1069Q mutation in East German patients with Wilson disease: rapid detection of mutations by limited sequencing and phenotype–genotype analysis-Reference-Cited by-同舟云学术

High prevalence of the H1069Q mutation in East German patients with Wilson disease: rapid detection of mutations by limited sequencing and phenotype–genotype analysis

Published:2001-11 Issue:5 Volume:35 Page:575-581
ISSN:0168-8278
Container-title:Journal of Hepatology
language:en
Short-container-title:Journal of Hepatology

Author:

Caca Karel,Ferenci Peter,Kühn Hans-Jürgen,Polli Claudia,Willgerodt Helmut,Kunath Bernhard,Hermann Wieland,Mössner Joachim,Berr Frieder

Publisher

Elsevier BV

Subject

Hepatology

Reference35 articles.

1. Perspectives on Wilson's disease;Sternlieb;Hepatology,1990

2. Wilson's disease;Scheinberg,1984

3. Wilson's disease in East Germany: in retrospect and perspectives – an evaluation;Lossner;Psychiatr Neurol Med Psychol,1990

4. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene;Tanzi;Nat Genet,1993

5. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene;Bull;Nat Genet,1993

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