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Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development
Gene abnormalities in RBFOX1, encoding an mRNA-splicing factor, have been shown to cause autism spectrum disorder and other neurodevelopmental disorders. Since pathophysiological significance of the dominant nuclear isoform in neurons, RBFOX1-isoform1 (iso1), remains to be elucidated, we performed c...
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| Yayımlandı: | Sci Rep |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Nature Publishing Group
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4969621/ https://ncbi.nlm.nih.gov/pubmed/27481563 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep30805 |
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