Mutation of a potassium channel–related
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Patrick Van Bogaert; Regis Azizieh; Julie Désir; Alec Aeby; Linda De Meirleir; J
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Article
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2007
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John Wiley and Sons
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English
⚖ 725 KB
## 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