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 wet[ recognised but the mechanism of inheritance and the genes involved are yet to be fully established.

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14 / Chioza BA; Aicardi J; Aschauer H; Brouwer O; Callenbach P; Covanis A; Dooley JM; Dulac O; Durner M; Eeg-Olofsson O; Feucht M; Friis ML; Guerrini R; Kjeldsen MJ; Nabbout R; Nashef L; Sander T; Sirén A; Wirrell E; McKeigue P; Robinson R; Gardiner RM; Everett KV.. - In: EPILEPSY RESEARCH. - ISSN 0920-1211. - STAMPA. - 87:(2009), pp. 247-255. [10.1016/j.eplepsyres.2009.09.010]

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

GUERRINI, RENZO;
2009

Abstract

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 wet[ recognised but the mechanism of inheritance and the genes involved are yet to be fully established.
2009
87
247
255
Chioza BA; Aicardi J; Aschauer H; Brouwer O; Callenbach P; Covanis A; Dooley JM; Dulac O; Durner M; Eeg-Olofsson O; Feucht M; Friis ML; Guerrini R; Kjeldsen MJ; Nabbout R; Nashef L; Sander T; Sirén A; Wirrell E; McKeigue P; Robinson R; Gardiner RM; Everett KV.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/375471
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