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Autism-associated mutation inhibits protein kinase C-mediated neuroligin-4X enhancement of excitatory synapses
Autism spectrum disorders (ASDs) comprise a highly heritable, multifarious group of neurodevelopmental disorders, which are characterized by repetitive behaviors and impairments in social interactions. Point mutations have been identified in X-linked Neuroligin (NLGN) 3 and 4X genes in patients with...
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| 出版年: | Proc Natl Acad Sci U S A |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4345621/ https://ncbi.nlm.nih.gov/pubmed/25675530 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1500501112 |
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