The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis-Reference-Cited by-同舟云学术

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis

Published:2004-11 Issue:5 Volume:41 Page:758-763
ISSN:0168-8278
Container-title:Journal of Hepatology
language:en
Short-container-title:Journal of Hepatology

Author:

Stapelbroek Janneke M.,Bollen Casper W.,Ploos van Amstel Johannes K.,van Erpecum Karel J.,van Hattum Jan,van den Berg Leonard H.,Klomp Leo W.J.,Houwen Roderick H.J.

Publisher

Elsevier BV

Subject

Hepatology

Reference37 articles.

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

3. The Wilson's disease gene and phenotypic diversity;Riordan;J Hepatol,2001

4. 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

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