Spinocerebellar ataxia type 6: founder effect in Western Japan
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference21 articles.
1. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1;Orr;Nat. Genet.,1993
2. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2;Pulst;Nat. Genet.,1996
3. CAG expansion in a novel gene for Machado–Joseph disease at chromosome 14q32.1;Kawaguchi;Nat. Genet.,1994
4. Dentatorubral and pallidoluysian atrophy expansion of unstable CAG trinucleotide on chromosome 12p;Nagafuchi;Nat. Genet.,1994
5. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel;Zhuchenko;Nat. Genet.,1997
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1. Population genetics of spinoсerebellar ataxias caused by polyglutamine expansions;Vavilov Journal of Genetics and Breeding;2019-07-07
2. Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome?;European Journal of Human Genetics;2008-02-20
3. Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population;Human Genetics;2005-04-20
4. Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations;European Journal of Human Genetics;2004-03-17
5. A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in Western Japan;Neuroscience Letters;2004-03
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