Functional genetic analysis of mutations implicated in a human speech and language disorder.

Functional genetic analysis of mutations implicated in a human speech and language disorder.

Mutations in the FOXP2 gene cause a severe communication disorder involving speech deficits (developmental verbal dyspraxia), accompanied by wide-ranging impairments in expressive and receptive language. The protein encoded by FOXP2 belongs to a divergent subgroup of forkhead-box transcription facto...

Descripción completa

Detalles Bibliográficos
Autores principales: Vernes, S, Nicod, J, Elahi, F, Coventry, J, Kenny, N, Coupe, A, Bird, L, Davies, K, Fisher, S
Formato: Journal article
Lenguaje:English
Publicado: 2006

Ejemplares similares

Ejemplares similares