Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD

Journal of Neural Transmission

Volumn 119, Issue 6, 2012, Pages 729-733

  Salatino Oliveira, Angélica ^a   Genro, Julia P ^a   Guimarães, Ana P ^a   Chazan, Rodrigo ^b   Zeni, Cristian ^b   Schmitz, Marcelo ^b   Polanczyk, Guilherme ^b,c   Roman, Tatiana ^a   Rohde, Luis A ^b,c   Hutz, Mara H ^a  

^a FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

^b HOSPITAL DE CLÍNICAS DE PORTO ALEGRE   (Brazil)

^c Instituto Nacional de Psiquiatria Do Desenvolvimento Para A Infância e Adolescência   (Brazil)

Author keywords

ADHD; CD; DBD; ODD; Val158Met

Indexed keywords

CATECHOL METHYLTRANSFERASE; METHIONINE; VALINE;

ADOLESCENT DISEASE; ARTICLE; ATTENTION DEFICIT DISORDER; CHILD; CHILDHOOD DISEASE; DISEASE ASSOCIATION; DISRUPTIVE BEHAVIOR; FEMALE; GENETIC POLYMORPHISM; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ALLELES; AMINO ACID SUBSTITUTION; ATTENTION DEFICIT AND DISRUPTIVE BEHAVIOR DISORDERS; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; BRAZIL; CATECHOL O-METHYLTRANSFERASE; CHILD; COMORBIDITY; CONDUCT DISORDER; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; DNA; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; MALE; NEUROPSYCHOLOGICAL TESTS; POLYMORPHISM, GENETIC; VALINE;

EID: 84863497183     PISSN: 03009564     EISSN: 14351463     Source Type: Journal    
DOI: 10.1007/s00702-012-0766-2     Document Type: Article

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