The norepinephrine transporter gene and attention-deficit hyperactivity disorder

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 114, Issue 3, 2002, Pages 255-259

  Barr, Cathy L ^a,b   Kroft, Jamie ^a   Feng, Yu ^a   Wigg, Karen ^a   Roberts, Wendy ^b   Malone, Molly ^b   Ickowicz, Abel ^b   Schachar, Russell ^b   Tannock, Rosemary ^b   Kennedy, James L ^c  

^a TORONTO WESTERN HOSPITAL   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

Author keywords

Attention deficit hyperactivity disorder; Genetics; Linkage; Norepinephrine transporter; Polymorphism; Transmission disequilibrium test

Indexed keywords

ATOMOXETINE; ISOLEUCINE; NORADRENALIN; SEROTONIN UPTAKE INHIBITOR; THREONINE;

ADRENERGIC SYSTEM; ALLELE; AMINO ACID ANALYSIS; ARTICLE; ATTENTION DEFICIT DISORDER; CHILD; CONTROLLED STUDY; DISEASE MODEL; EXON; GENE FREQUENCY; GENE ISOLATION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; INHERITANCE; INTRON; MAJOR CLINICAL STUDY; NET1 GENE; NORADRENALIN RELEASE; PHENOTYPE; PRIORITY JOURNAL;

ALLELES; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GENE FREQUENCY; HUMANS; MALE; MUTATION, MISSENSE; NOREPINEPHRINE PLASMA MEMBRANE TRANSPORT PROTEINS; POINT MUTATION; SYMPORTERS;

ANIMALIA;

EID: 0037041305     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.10193     Document Type: Article

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