Article
Channelopathies as a genetic cause of epilepsy
2003-04-01
Abstract excerpt
Purpose of review This review describes the significant number of new gene associations with epilepsy syndromes that have emerged during the past year, together with additional mutations and new electrophysiological data relating to previously known gene associations. Recent findings Autosomal dominant juvenile myoclonic epilepsy was demonstrated to be a channelopathy associated with a GABAA receptor, α1 subunit m...
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Identifiers and source
- Literature Corpus work
- 8a5181b0-2245-5764-945c-3d41a69bb093
- DOI
- 10.1097/00019052-200304000-00009