Functional significance of rare neuroligin 1 variants found in autism

Genetic mutations contribute to the etiology of autism spectrum disorder (ASD), a common, heterogeneous neurodevelopmental disorder characterized by impairments in social interaction, communication, and repetitive and restricted patterns of behavior. Since neuroligin3 (NLGN3), a cell adhesion molecu...

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Dades bibliogràfiques
Publicat a:PLoS Genet
Autors principals: Nakanishi, Moe, Nomura, Jun, Ji, Xiao, Tamada, Kota, Arai, Takashi, Takahashi, Eiki, Bućan, Maja, Takumi, Toru
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2017
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5571902/
https://ncbi.nlm.nih.gov/pubmed/28841651
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006940
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