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CAG repeat expansions in patients with sporadic cerebellar ataxia

✍ Scribed by N. Futamura; R. Matsumura; Y. Fujimoto; H. Horikawa; A. Suzumura; T. Takayanagi


Book ID
109336878
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
553 KB
Volume
98
Category
Article
ISSN
0001-6314

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Autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders that generally present in adulthood. Spinocerebellar ataxia type 2 typically presents with progressive cerebellar symptoms, slow ocular saccades, and peripheral neuropathy. The onset of symptoms is usually