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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Bibliographic Details
Main Authors: Martine eHoogman, Tulio eGuadalupe, Marcel Peter Zwiers, Patricia eKlarenbeek, Clyde eFrancks, Simon Edward Fisher
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-07-01
Series:Frontiers in Human Neuroscience
Subjects:
VBM
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnhum.2014.00473/full