Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.

doi:10.1016/j.eplepsyres.2009.09.010

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Article

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.

Epilepsy research - 1 Dec 2009

Chioza Barry A, Aicardi Jean, Aschauer Harald, Brouwer Oebele, Callenbach Petra, Covanis Athanasios, Dooley Joseph M, Dulac Olivier, Durner Martina, Eeg-Olofsson Orvar, Feucht Martha, Friis Mogens Laue, Guerrini Renzo, Kjeldsen Marianne Juel, Nabbout Rima, Nashef Lina, Sander Thomas, Sirén Auli, Wirrell Elaine, McKeigue Paul, Robinson Robert, Gardiner R Mark, Everett Kate V

Abstract excerpt

Childhood absence epilepsy (CAE) is an idiopathic generalised epilepsy (IGE) characterised by typical absence seizures manifested by transitory loss of awareness with 2.5-4 Hz spike-wave complexes on ictal EEG. A genetic component to the aetiology is well recognised but the mechanism of inheritance and the genes involved are yet to be fully established. A genome wide single nucleotide polymorphism (SNP)-based...

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PMID: 19837565
DOI: 10.1016/j.eplepsyres.2009.09.010
PMCID: PMC2791882

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