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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Bibliographic Details
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.
Format: Artigo
Language:Inglês
Published: 2011
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Article
Online Access: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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