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pubmed-article:19401771pubmed:abstractTextMotor deficits are a critical component of the clinical characteristics of patients with spinocerebellar ataxia type 2. However, there is no current information on the preclinical manifestation of those motor deficits in presymptomatic gene carriers. To further understand and characterize the onset of the clinical manifestation in this disease, we tested presymptomatic spinocerebellar ataxia type 2 gene carriers, and volunteers, in a task that evaluates their motor performance and their motor learning capabilities.lld:pubmed
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pubmed-article:19401771pubmed:articleTitleMotor decline in clinically presymptomatic spinocerebellar ataxia type 2 gene carriers.lld:pubmed
pubmed-article:19401771pubmed:affiliationCentro para la Investigación y Rehabilitación de las Ataxias Hereditarias, Holguín, Cuba.lld:pubmed
pubmed-article:19401771pubmed:publicationTypeJournal Articlelld:pubmed
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