Abstract:
: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.
journal_name
Neurologyjournal_title
Neurologyauthors
Storey E,Gardner RJ,Knight MA,Kennerson ML,Tuck RR,Forrest SM,Nicholson GAdoi
10.1212/wnl.57.10.1913subject
Has Abstractpub_date
2001-11-27 00:00:00pages
1913-5issue
10eissn
0028-3878issn
1526-632Xjournal_volume
57pub_type
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