Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

The epilepsies are a common, clinically heterogeneous group of disorders defined by recurrent unprovoked seizures1. Here we describe identification of the causative gene in autosomal-dominant partial epilepsy with auditory features (ADPEAF, MIM 600512), a rare form of idiopathic lateral temporal lob...

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Detalhes bibliográficos
Main Authors: Kalachikov, Sergey, Evgrafov, Oleg, Ross, Barbara, Winawer, Melodie, Barker-Cummings, Christie, Boneschi, Filippo Martinelli, Choi, Chang, Morozov, Pavel, Das, Kamna, Teplitskaya, Elita, Yu, Andrew, Cayanis, Eftihia, Penchaszadeh, Graciela, Kottmann, Andreas H., Pedley, Timothy A., Hauser, W. Allen, Ottman, Ruth, Gilliam, T. Conrad
Formato: Artigo
Idioma:Inglês
Publicado em: 2002
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2606053/
https://ncbi.nlm.nih.gov/pubmed/11810107
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng832
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