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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Hoogman, Martine, Guadalupe, Tulio, Zwiers, Marcel P., Klarenbeek, Patricia, Francks, Clyde, Fisher, Simon E.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2014
Pynciau:
Mynediad Ar-lein: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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