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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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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2014
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| 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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