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Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1

✍ Scribed by Dr Sinan Çomu; Vinodh Narayanan; Michael Giuliani

Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
338 KB
Volume
40
Category
Article
ISSN
0364-5134

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Mutation of a potassium channel–related
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## Abstract ## Objective We investigated a large consanguineous Moroccan family with progressive myoclonic epilepsy (PME) consistent with autosomal recessive inheritance, to describe the phenotype and identify the causal gene. ## Methods We recorded the clinical course of the disease and the res