Mutations in GABA(A) receptor subunits associated with genetic epilepsies

Mutations in inhibitory GABA(A) receptor subunit genes (GABRA1, GABRB3, GABRG2 and GABRD) have been associated with genetic epilepsy syndromes including childhood absence epilepsy (CAE), juvenile myoclonic epilepsy (JME), pure febrile seizures (FS), generalized epilepsy with febrile seizures plus (G...

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Detalhes bibliográficos
Main Authors: Macdonald, Robert L, Kang, Jing-Qiong, Gallagher, Martin J
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2010
Assuntos:
Special Section Reviews: Neurological Channelopathies
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2901974/
https://ncbi.nlm.nih.gov/pubmed/20308251
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2010.186999
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