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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Detalles Bibliográficos
Autores principales: Becker, Martin, Devanna, Paolo, Fisher, Simon E., Vernes, Sonja C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826363/
https://www.ncbi.nlm.nih.gov/pubmed/29515369
http://dx.doi.org/10.3389/fnmol.2018.00047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826363/
https://www.ncbi.nlm.nih.gov/pubmed/29515369
http://dx.doi.org/10.3389/fnmol.2018.00047

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