Association of genetic variants of GRIN2B with autism

Scientific Reports

Volumn 5, Issue , 2015, Pages

  Pan, Yongcheng ^a   Chen, Jingjing ^a   Guo, Hui ^a,b   Ou, Jianjun ^b   Peng, Yu ^a   Liu, Qiong ^a   Shen, Yidong ^b   Shi, Lijuan ^b   Liu, Yalan ^a,c   Xiong, Zhimin ^a   Zhu, Tengfei ^a   Luo, Sanchuan ^a   Hu, Zhengmao ^a   Zhao, Jingping ^a,b   Xia, Kun ^a,d  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b CENTRAL SOUTH UNIVERSITY   (China)

^c CENTRAL SOUTH UNIVERSITY   (China)

^d XINJIANG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

N METHYL DEXTRO ASPARTIC ACID RECEPTOR; NR2B NMDA RECEPTOR;

ALLELE; AMINO ACID SUBSTITUTION; AUTISM; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENETICS; HAPLOTYPE; HUMAN; ODDS RATIO; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; AMINO ACID SUBSTITUTION; AUTISTIC DISORDER; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, N-METHYL-D-ASPARTATE;

EID: 84954305553     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep08296     Document Type: Article

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