Polymorphisms in the TSHR (thyrotropin receptor) gene on chromosome 14q31 are not associated with mental retardation in the iodine-deficient areas of China

Neuroscience Letters

Volumn 382, Issue 1-2, 2005, Pages 179-184

  Guo, Ting Wei ^a,b   Zhang, Fu Chang ^c   Gao, Jian Jun ^a,b   Bian, Li ^a,b   Gao, Xiao Cai ^c   Ma, Jie ^a,b   Yang, Maosheng ^a,b   Ji, Qian ^a,b   Duan, Shi Wei ^a,b   Zheng, Zi Jian ^c   Li, Rui Lin ^d   Feng, Guo Yin ^e   St Clair, David ^b,f   He, Lin ^b,g  

^a Chinese Academy of Sciences   (China)

^b SHANGHAI JIAO TONG UNIVERSITY   (China)

^c NORTHWEST UNIVERSITY   (China)

^d XI'AN JIAOTONG UNIVERSITY   (China)

^e SHANGHAI MENTAL HEALTH CENTER   (China)

^f UNIVERSITY OF ABERDEEN   (United Kingdom)

^g INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

Author keywords

Haplotype; Linkage disequilibrium; Mental retardation (MR); Thyroid hormone; TSHR (thyrotropin receptor)

Indexed keywords

THYROID HORMONE; THYROTROPIN; THYROTROPIN RECEPTOR;

ARTICLE; CHINA; CHROMOSOME 14Q; CONTROLLED STUDY; DNA POLYMORPHISM; GENE LINKAGE DISEQUILIBRIUM; GENETIC ANALYSIS; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; IODINE DEFICIENCY; MENTAL DEFICIENCY; PRIORITY JOURNAL;

ALLELES; CHILD; CHINA; CHROMOSOMES, HUMAN, PAIR 14; CONGENITAL HYPOTHYROIDISM; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; IODINE; LINKAGE DISEQUILIBRIUM; MALE; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, THYROTROPIN; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 19544393197     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2005.03.007     Document Type: Article

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