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The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
Rare disruptions of FOXP2 have been strongly implicated in deficits in language development. Research over the past decade has suggested a role in the formation of underlying neural circuits required for speech. Until recently no evidence existed to suggest that the closely related FOXP1 gene played...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer-Verlag
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470686/ https://www.ncbi.nlm.nih.gov/pubmed/22736078 http://dx.doi.org/10.1007/s00439-012-1193-z |