Neurogenetics and auditory processing in developmental dyslexia

被引：80

作者：

Giraud, Anne-Lise ^{[1
,2
]}

Ramus, Franck ^{[3
]}

机构：

[1] Ecole Normale Super, INSERM, Dept Etud Cognit, U960, F-75005 Paris, France

[2] Univ Geneva, Dept Neurosci, CH-1211 Geneva 4, Switzerland

[3] CNRS, EHESS, Ecole Normale Super, Lab Sci Cognit & Psycholinguist, F-75005 Paris, France

来源：

CURRENT OPINION IN NEUROBIOLOGY | 2013年 / 23卷 / 01期

关键词：

IN-UTERO RNAI; BEHAVIORAL IMPAIRMENTS; SUSCEPTIBILITY GENE; CANDIDATE GENES; SPEECH; BRAIN; DCDC2; KIAA0319; CHILDREN; SKILLS;

D O I：

10.1016/j.conb.2012.09.003

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

Dyslexia is a polygenic developmental reading disorder characterized by an auditory/phonological deficit. Based on the latest genetic and neurophysiological studies, we propose a tentative model in which phonological deficits could arise from genetic anomalies of the cortical micro-architecture in the temporal lobe.

引用

收藏

页码：37 / 42

页数：6

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