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...

Полное описание

Библиографические подробности
Главные авторы:	Vernes, S, Nicod, J, Elahi, F, Coventry, J, Kenny, N, Coupe, A, Bird, L, Davies, K, Fisher, S
Формат:	Journal article
Язык:	English
Опубликовано:	2006

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