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FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways

FOXP2 was the first gene shown to cause a Mendelian form of speech and language disorder. Although developmentally expressed in many organs, loss of a single copy of FOXP2 leads to a phenotype that is largely restricted to orofacial impairment during articulation and linguistic processing deficits....

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Detalhes bibliográficos
Main Authors: Devanna, Paolo, Middelbeek, Jeroen, Vernes, Sonja C.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4176457/
https://ncbi.nlm.nih.gov/pubmed/25309332
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2014.00305
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