Early neuroimaging markers of FOXP2 intragenic deletion

FOXP2 is the major gene associated with severe, persistent, developmental speech and language disorders. While studies in the original family in which a FOXP2 mutation was found showed volume reduction and reduced activation in core language and speech networks, there have been no imaging studies of...

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Detalles Bibliográficos
Autores principales: Liégeois, Frédérique J., Hildebrand, Michael S., Bonthrone, Alexandra, Turner, Samantha J., Scheffer, Ingrid E., Bahlo, Melanie, Connelly, Alan, Morgan, Angela T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062117/
https://www.ncbi.nlm.nih.gov/pubmed/27734906
http://dx.doi.org/10.1038/srep35192

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062117/
https://www.ncbi.nlm.nih.gov/pubmed/27734906
http://dx.doi.org/10.1038/srep35192

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