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...

詳細記述

書誌詳細
主要な著者: Vernes, S, Nicod, J, Elahi, F, Coventry, J, Kenny, N, Coupe, A, Bird, L, Davies, K, Fisher, S
フォーマット: Journal article
言語:English
出版事項: 2006