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
收藏
页码：177 / 207
页数：31
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