About the meaning of FOXP2 gene discovery

被引：0

作者：

Longa, Victor M. ^{[1
]}

机构：

[1] Univ Santiago Compostela, Santiago De Compostela, Spain

来源：

ESTUDIOS DE LINGUISTICA-UNIVERSIDAD DE ALICANTE-ELUA | 2006年 / 20期

关键词：

F0XP2; language; cognitive genetics; Specific Language Impairment; Minimalist Program;

D O I：

10.14198/ELUA2006.20.09

中图分类号：

H [语言、文字];

学科分类号：

05 ;

摘要：

The recent discovery of the FOXP2 gene has provided us with the first clear evidence of the genetic basis of language. Such a discovery has shown an unmistakable genetic correlation between a mutated version of F0XP2 and several linguistic impairments suffered by an English family, named KE. The main objective of this arricie is to discuss a number of topics concerning the aforementioned discovery. More specifically, the paper aims at discussing the significance of F0X2 with regard to language and language development.

引用

页码：177 / 207

页数：31

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