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Assessing the effects of common variation in the FOXP2 gene on human brain structure
The FOXP2 transcription factor is one of the most well-known genes to have been implicated in developmental speech and language disorders. Rare mutations disrupting the function of this gene have been described in different families and cases. In a large three-generation family carrying a missense m...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076884/ https://www.ncbi.nlm.nih.gov/pubmed/25013396 http://dx.doi.org/10.3389/fnhum.2014.00473 |