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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...
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| Main Authors: | , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Frontiers Media S.A.
2014
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4076884/ https://ncbi.nlm.nih.gov/pubmed/25013396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnhum.2014.00473 |
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