Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities and core autism-related deficits

Although many genes predisposing to autism spectrum disorders (ASD) have been identified, the biological mechanism(s) remain unclear. Mouse models based on human disease-causing mutations provide the potential for understanding gene function and novel treatment development. Here we characterize a mo...

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Main Authors: Peñagarikano, Olga, Abrahams, Brett S., Herman, Edward I., Winden, Kellen C., Gdalyahu, Amos, Dong, Hongmei, Sonnenblick, Lisa I., Gruver, Robin, Almajano, Joel, Bragin, Anatol, Golshani, Peyman, Trachtenberg, Joshua T., Peles, Elior, Geschwind, Daniel H.
Formato: Artigo
Idioma:Inglês
Publicado: 2011
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3390029/
https://ncbi.nlm.nih.gov/pubmed/21962519
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2011.08.040
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