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Article

Channelopathies as a genetic cause of epilepsy.

Current opinion in neurology - 1 Apr 2003

Mulley John C, Scheffer Ingrid E, Petrou Steven, Berkovic Samuel F

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 GABA(A) receptor, alpha1...

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Identifiers

PMID: 12644745
DOI: 10.1097/01.wco.0000063767.15877.c7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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