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Mapping of Human FOXP2 Enhancers Reveals Complex Regulation
Mutations of the FOXP2 gene cause a severe speech and language disorder, providing a molecular window into the neurobiology of language. Individuals with FOXP2 mutations have structural and functional alterations affecting brain circuits that overlap with sites of FOXP2 expression, including regions...
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| Publicado no: | Front Mol Neurosci |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5826363/ https://ncbi.nlm.nih.gov/pubmed/29515369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2018.00047 |
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