Linkage and association analysis of CACNG3 in childhood absence epilepsy

Childhood absence epilepsy (CAE) is an idiopathic generalised epilepsy characterised by absence seizures manifested by transitory loss of awareness with 2.5-4Hz spike-wave complexes on ictal EEG. A genetic component to aetiology is established but the mechanism of inheritance and the genes involved...

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Detalhes bibliográficos
Main Authors: Everett, Kate, Chioza, Barry, Aicardi, Jean, Aschauer, Harald, Brouwer, Oebele, Callenbach, Petra, Covanis, Athanasios, Dulac, Olivier, Eeg-Olofsson, Orvar, Feucht, Martha, Friis, Mogens, Goutieres, Françoise, Guerrini, Renzo, Heils, Armin, Kjeldsen, Marianne, Lehesjoki, Anna-Elina, Makoff, Andrew, Nabbout, Rima, Olsson, Ingrid, Sander, Thomas, Sirén, Auli, McKeigue, Paul, Robinson, Robert, Taske, Nichole, Rees, Michele, Gardiner, Mark
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2556708/
https://ncbi.nlm.nih.gov/pubmed/17264864
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201783
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