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Spontaneous and induced mouse mutations with cerebellar dysfunctions: Behavior and neurochemistry

✍ Scribed by R. Lalonde; C. Strazielle

Book ID
113501350
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
934 KB
Volume
1140
Category
Article
ISSN
0006-8993

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## Abstract Episodic Ataxia Type 1 is an autosomal dominant disorder characterized by episodes of ataxia and myokymia. It is associated with mutations in the __KCNA1__ voltage‐gated potassium channel gene. In the present study, we describe a family with novel clinical features including persistent