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2007•Epilepsy ResearchRequires access

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy

Anne Hempelmann, Joana Cobilanschi, Armin Heils, Hiltrud Muhle, Ulrich Stephani, Yvonne Weber, Holger Lerche, Thomas Sander

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Key concepts: Juvenile myoclonic epilepsy, Idiopathic generalized epilepsy, Childhood absence epilepsy, Epilepsy, Allele, Single-nucleotide polymorphism, Genetics, Linkage disequilibrium

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Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy — Research Paper | ScholarLens