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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Príomhchruthaitheoirí: Argyropoulos, G, Watkins, K, Belton- Pagnamenta, E, Liégeois, F, Saleem, K, Mishkin, M, Vargha-Khadem, F
Formáid: Journal article
Foilsithe / Cruthaithe: Springer US 2018