Association of genetic variants of GRIN2B with autism

Autism (MIM 209850) is a complex neurodevelopmental disorder characterized by social communication impairments and restricted repetitive behaviors. It has a high heritability, although much remains unclear. To evaluate genetic variants of GRIN2B in autism etiology, we performed a system association...

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Bibliografiska uppgifter
I publikationen:Sci Rep
Huvudupphovsmän: Pan, Yongcheng, Chen, Jingjing, Guo, Hui, Ou, Jianjun, Peng, Yu, Liu, Qiong, Shen, Yidong, Shi, Lijuan, Liu, Yalan, Xiong, Zhimin, Zhu, Tengfei, Luo, Sanchuan, Hu, Zhengmao, Zhao, Jingping, Xia, Kun
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group 2015
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4319152/
https://ncbi.nlm.nih.gov/pubmed/25656819
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep08296
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