Neocerebellar Crus I Abnormalities Associated with a Speech and Language Disorder Due to a Mutation in FOXP2

Bilateral volume reduction in the caudate nucleus has been established as a prominent brain abnormality associated with a FOXP2 mutation in affected members of the ‘KE family’, who present with developmental orofacial and verbal dyspraxia in conjunction with pervasive language deficits. Despite the...

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Detalles Bibliográficos
Autores principales: Argyropoulos, G. P. D., Watkins, K. E., Belton-Pagnamenta, E., Liégeois, F., Saleem, K. S., Mishkin, M., Vargha-Khadem, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517346/
https://www.ncbi.nlm.nih.gov/pubmed/30460543
http://dx.doi.org/10.1007/s12311-018-0989-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517346/
https://www.ncbi.nlm.nih.gov/pubmed/30460543
http://dx.doi.org/10.1007/s12311-018-0989-3

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