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pubmed-article:16078202pubmed:abstractTextWe have assessed the haplotypes at the ATXN2 locus in Taiwanese controls and in individuals with SCA2 ataxia with both ataxic and parkinsonian features. Our intention was to determine whether a different ataxin 2 haplotypes predisposed to the two phenotypes. In fact, our analysis showed that all SCA2 mutations carriers had the same ataxin 2 haplotype: haplotype B, which accounts for only 15% of control haplotypes, implying that there is a common founder for all Taiwanese SCA2 patients.lld:pubmed
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pubmed-article:16078202pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:16078202pubmed:articleTitleTaiwanese cases of SCA2 are derived from a single founder.lld:pubmed
pubmed-article:16078202pubmed:affiliationLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland 20952, USA. momeni@mail.nih.govlld:pubmed
pubmed-article:16078202pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16078202pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:16078202pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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