Article
Screening of GABRB3 in French-Canadian families with idiopathic generalized epilepsy.
Epilepsia - 1 Sept 2010
Lachance-Touchette Pamela, Martin Caroline, Poulin Chantal, Gravel Micheline, Carmant Lionel, Cossette Patrick
Abstract excerpt
Mutations in the GABRB3 have been recently associated with childhood absence epilepsy (CAE) in families from Honduras and Mexico. In this study, we aimed to determine the frequency of mutation in this gene in our cohort of families with CAE and other related idiopathic generalized epilepsy (IGE)...
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