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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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| Publicado no: | PLoS Genet |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2017
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| Assuntos: | |
| Acesso em linha: | 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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