A Family-based Association Study of DIO2 and children mental retardation in the Qinba region of China

Journal of Human Genetics

Volumn 57, Issue 1, 2012, Pages 14-17

  Zhang, Kejin ^a   Xi, Heng ^a,b   Wang, Xiying ^a   Guo, Yale ^c   Huang, Shaoping ^c   Zheng, Zijian ^b   Zhang, Fuchang ^a,b   Gao, Xiaocai ^a,b  

^a BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

^b NORTHWEST UNIVERSITY   (China)

^c XI'AN JIAOTONG UNIVERSITY   (China)

Author keywords

deiodinase enzyme II (DIO2); Family Based Association Tests (FBAT); mental retardation (MR); thyroid hormone (TH)

Indexed keywords

IODIDE PEROXIDASE; IODIDE PEROXIDASE II; UNCLASSIFIED DRUG;

ARTICLE; CHILD; CHINA; COMPUTER MODEL; FAMILY; GENE EXPRESSION; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC SUSCEPTIBILITY; GENOTYPE; HAPLOTYPE; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; PEDIGREE; RELATIVE; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHINA; FAMILY; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; INTELLECTUAL DISABILITY; IODIDE PEROXIDASE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84863052450     PISSN: 14345161     EISSN: 1435232X     Source Type: Journal    
DOI: 10.1038/jhg.2011.121     Document Type: Article

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