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

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...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science Publishers 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2791882/
https://www.ncbi.nlm.nih.gov/pubmed/19837565
http://dx.doi.org/10.1016/j.eplepsyres.2009.09.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2791882/
https://www.ncbi.nlm.nih.gov/pubmed/19837565
http://dx.doi.org/10.1016/j.eplepsyres.2009.09.010

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