Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population

BACKGROUND: Dyslexia is a polygenic developmental disorder characterized by difficulties in reading and spelling despite normal intelligence, educational backgrounds and perception. Increasing evidences indicated that dyslexia may share similar genetic mechanisms with other speech and language disor...

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Detaylı Bibliyografya
Yayımlandı:Behav Brain Funct
Asıl Yazarlar: Chen, Huan, Wang, Guoqing, Xia, Jiguang, Zhou, Yuxi, Gao, Yong, Xu, Junquan, Huen, Michael SY, Siok, Wai Ting, Jiang, Yuyang, Tan, Li Hai, Sun, Yimin
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2014
Konular:
Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4236612/
https://ncbi.nlm.nih.gov/pubmed/25178928
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-10-29
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