Lack of association between polymorphism-592A/C in the promoter region of the IL10 gene and tourette's syndrome in a family-based association study in the Chinese han population

Genetic Testing and Molecular Biomarkers

Volumn 15, Issue 10, 2011, Pages 733-735

  Liu, Shiguo ^a   Yi, Mingji ^a   Qi, Fengguang ^a   Che, Fengyuan ^b   Ma, Xu ^c,d,e  

^a QINGDAO UNIVERSITY   (China)

^b SHANDONG UNIVERSITY   (China)

^c GRADUATE SCHOOL OF PEKING UNION MEDICAL COLLEGE   (China)

^d NATIONAL RESEARCH INSTITUTE FOR FAMILY PLANNING   (China)

^e WORLD HEALTH ORGANIZATION   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

INTERLEUKIN 10;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINESE; DISEASE ASSOCIATION; DNA POLYMORPHISM; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC RISK; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HAPLOTYPE; HUMAN; IN VIVO STUDY; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PROMOTER REGION; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; FAMILY; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETICS, POPULATION; HUMANS; INTERLEUKIN-10; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC; TOURETTE SYNDROME;

EID: 80054697813     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2010.0272     Document Type: Article

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