A new autosomal dominant pure cerebellar ataxia.

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

Neurology

journal_title

Neurology

authors

Storey E,Gardner RJ,Knight MA,Kennerson ML,Tuck RR,Forrest SM,Nicholson GA

doi

10.1212/wnl.57.10.1913

subject

Has Abstract

pub_date

2001-11-27 00:00:00

pages

1913-5

issue

10

eissn

0028-3878

issn

1526-632X

journal_volume

57

pub_type

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