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JOURNAL ARTICLE
RESEARCH SUPPORT, NON-U.S. GOV'T
A new autosomal dominant pure cerebellar ataxia.
Neurology 2001 November 28
A kindred is described with a dominantly inherited "pure" cerebellar ataxia in which the currently known spinocerebellar ataxias have been excluded. In the eight subjects studied, a notable clinical feature is slow progression, with the three least affected having only a mild degree of gait ataxia after three or more decades of disease duration. Pending an actual chromosomal locus discovery, the name spinocerebellar ataxia (SCA)15 is expectantly applied.
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