Article
Frequency of His1069Gln and Gly1267Lys mutations in Polish Wilson's disease population.
European journal of neurology - 1 Sept 2000
Tarnacka B, Gromadzka G, Rodo M, Mierzejewski P, Czloonkowska A
Abstract excerpt
Wilson's disease is an autosomal recessive disorder. More than 60 mutations of the Wilson's disease gene have been described so far. We have analysed 148 Polish Wilson's disease patients from 95 families for His1069Gln and Gly1267Lys mutations and correlated this finding with age and clinical form of the disease at presentation. To identify these mutations, single strand conformation polymorphism analysis was...
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