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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2018-02-01
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| Col·lecció: | Frontiers in Molecular Neuroscience |
| Matèries: | |
| Accés en línia: | http://journal.frontiersin.org/article/10.3389/fnmol.2018.00047/full |
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