Families with Wilson's disease in subsequent generations: Clinical and genetic analysis
Author:
Affiliation:
1. 2nd Department of Neurology; Institute of Psychiatry and Neurology; Warsaw Poland
2. Department of Clinical and Experimental Pharmacology; Medical University of Warsaw; Poland
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference40 articles.
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3. Monozygotic female twins discordant for phenotype of Wilson's disease;Członkowska;Mov Disord,2009
4. p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease;Gromadzka;Mov Disord,2006
5. The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease;Schiefermeier;Brain,2000
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