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A novel approach for treating cerebellar ataxias

✍ Scribed by Mario Manto; Nordeyn Oulad Ben Taib


Book ID
116744324
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
69 KB
Volume
71
Category
Article
ISSN
0306-9877

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## Abstract Episodic ataxia type 2 (EA2) is a dominantly inherited disorder, characterized by spells of ataxia, dysarthria, vertigo, and migraines, associated with mutations in the neuronal calcium‐channel gene __CACNA1A__. Ataxic spells lasting minutes to hours are provoked by stress, exercise, or