The monoamine oxidase B gene exhibits significant association to ADHD

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 147, Issue 3, 2008, Pages 370-374

  Li, Jun ^a,d   Wang, Yufeng ^a   Hu, Songnian ^b   Zhou, Rulun ^a   Yu, Xiaomin ^b   Wang, Bing ^a   Guan, Lili ^a   Yang, Li ^a   Zhang, Feng ^b   Faraone, Stephen V ^c  

^a PEKING UNIVERSITY SIXTH HOSPITAL   (China)

^b BGI SHENZHEN   (China)

^c SUNY UPSTATE MEDICAL UNIVERSITY   (United States)

^d BEIJING NORMAL UNIVERSITY   (China)

Author keywords

ADHD; Gene; Monoamine oxidase B; Sequence; X chromosome

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME B;

3' UNTRANSLATED REGION; ADOLESCENT; ARTICLE; ATTENTION DEFICIT DISORDER; CHINA; CHINESE; DNA FLANKING REGION; ENZYME DEGRADATION; EXON; FEMALE; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC LINKAGE; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEX DIFFERENCE; X CHROMOSOME;

ADOLESCENT; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; BASE SEQUENCE; CHILD; DNA PRIMERS; EXONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HAPLOTYPES; HUMANS; INTRONS; LINKAGE DISEQUILIBRIUM; MALE; MONOAMINE OXIDASE;

EID: 42149177789     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30606     Document Type: Article

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