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The FOXP2 transcription factor is one of the most well-known genes to have been implicated in developmental speech and language disorders. Rare mutations disrupting the function of this gene have been...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened up novel avenues for investigating the relevant neural pathways. FOXP2 shows remarkably high conser...
Forkhead box P2 (FOXP2) is a highly conserved transcription factor that has been implicated in human speech and language disorders and plays important roles in the plasticity of the developing brain. ...
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described examples of monogenic speech and language disorders. Acquisition of proficient spoken language involves aud...
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which have been best characterised in a large pedigree called the KE family. The encoded protein is highly ...
Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and language disorder. Aetiological mutations of murine Foxp2 yield abnormal synaptic plasticity and impaired motorskil...
FOXP2基因是人类发现的第一个与语言相关的基因。自其被发现二十多年来,它已经成为国外有关语言神经生物学和生物语言学研究的前言热点。本文根据FOXP2与语言相关性研究的历程和现状以及Kate Distin的模因观或文化DNA假说,初步分析了语言的起源、习得和进化过程。在此基础上,文章对Chomsky的"普遍语法"提出了一些质疑。

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