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Sumoylation of FOXP2 regulates motor function and vocal communication through Purkinje cell development
BACKGROUND: Mutations in the gene encoding the transcription factor forkhead box P2, FOXP2, result in brain developmental abnormalities including reduced gray matter in both human patients and rodent models, and speech and language deficits. However, neither the region-specific function of FOXP2 in...
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| Publicado no: | Biol Psychiatry |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4983264/ https://ncbi.nlm.nih.gov/pubmed/27009683 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2016.02.008 |
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