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- W2890724809 abstract "ABSTRACT Spinocerebellar ataxias (SCA) are a clinically and genetically heterogeneous group of monogenic diseases that share ataxia and autosomal dominant inheritance as the core features. An important proportion of SCAs are caused by CAG trinucleotide repeat expansions in the coding region of different genes. In addition to genetic heterogeneity, clinical features transcend motor symptoms, including cognitive, electrophysiological and imaging aspects. Despite all the progress in the past 25 years, the mechanisms that determine how neuronal death is mediated by these unstable expansions are still unclear. The aim of this article is to review, from an historical point of view, the first CAG-related ataxia to be genetically described: SCA 1." @default.
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- W2890724809 date "2018-08-01" @default.
- W2890724809 modified "2023-09-30" @default.
- W2890724809 title "Twenty-five years since the identification of the first SCA gene: history, clinical features and perspectives for SCA1" @default.
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- W2890724809 doi "https://doi.org/10.1590/0004-282x20180080" @default.
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