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Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV(+) Cortical Interneurons
Human mutations in CNTNAP2 are associated with an array of neuropsychiatric and neurological syndromes, including speech and language disorders, epilepsy, and autism spectrum disorder (ASD). We examined Cntnap2’s expression and function in GABAergic cortical interneurons (CINs), where its RNA is pre...
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| 出版年: | Cereb Cortex |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6455910/ https://ncbi.nlm.nih.gov/pubmed/29028946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhx248 |
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