Association between polymorphisms in serotonin 2C receptor gene and attention-deficit/hyperactivity disorder in Han Chinese subjects

Neuroscience Letters

Volumn 407, Issue 2, 2006, Pages 107-111

  Li, Jun ^a   Wang, Yufeng ^a   Zhou, Rulun ^a   Zhang, Haobo ^a   Yang, Li ^a   Wang, Bing ^a   Faraone, Stephen V ^b  

^a PEKING UNIVERSITY SIXTH HOSPITAL   (China)

^b State University of New York Upstate Medical University: College of Medicine   (United States)

Author keywords

ADHD; Gene; Haplotype; Linkage disequilibrium; Polymorphism; Receptor; Serotonin

Indexed keywords

SEROTONIN 2C RECEPTOR;

ADOLESCENT; ADULT; ALLELE; ARTICLE; ATTENTION DEFICIT DISORDER; CHILD; CHINESE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC TRAIT; HAPLOTYPE; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PRIORITY JOURNAL; RECEPTOR GENE;

ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD; CHINA; FEMALE; GENE FREQUENCY; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; POLYMORPHISM, GENETIC; PSYCHIATRIC STATUS RATING SCALES; RECEPTOR, SEROTONIN, 5-HT2C; SEX CHARACTERISTICS; X CHROMOSOME;

EID: 33748687580     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2006.08.022     Document Type: Article

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