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- W2048654851 abstract "In the past decade, genetics has propelled advances in neurology more than in any other medical discipline. Nowhere is this more apparent than in the study of hereditary ataxia. 1 Paulson H Ammache Z Ataxia and hereditary disorders. Neurel Clin. 2001; 19: 759-782 Summary Full Text Full Text PDF PubMed Scopus (41) Google Scholar Ataxias that were formerly lumped under imprecise clinicopathological labels, such as corticocerebellar atrophy and olivopontocerebellar atrophy, are now classified solely on the basis of their underlying genetic defects. For example, the expanding group of identified dominant ataxias—spinocerebellar ataxias (SCAs)—are assigned numbers as each new locus is mapped. Since the chromosomal mapping of the first SCA in 1990 (SCAl), the list has rapidly grown. Indeed, the list has reached the point where it bewilders even the specialist." @default.
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- W2048654851 date "2002-12-01" @default.
- W2048654851 modified "2023-09-27" @default.
- W2048654851 title "Yet another spinocerebellar ataxia—will it ever end?" @default.
- W2048654851 cites W1967286323 @default.
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- W2048654851 doi "https://doi.org/10.1016/s1474-4422(02)00234-x" @default.
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