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A Potassium Channel Mutation in Neonatal Human Epilepsy

✍ Scribed by Biervert, C.

Book ID
118274254
Publisher
American Association for the Advancement of Science
Year
1998
Tongue
English
Weight
613 KB
Volume
279
Category
Article
ISSN
0036-8075

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πŸ“œ SIMILAR VOLUMES

Mutation of a potassium channel–related
Mutation of a potassium channel–related gene in progressive myoclonic epilepsy
✍ Patrick Van Bogaert; Regis Azizieh; Julie DΓ©sir; Alec Aeby; Linda De Meirleir; J πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 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