Dopamine ß-hydroxylase gene associates with stroop color-word task performance in Han Chinese children with attention deficit/hyperactivity disorder.
Ji, Ning; Shuai, Lan; Chen, Yun; Liu, Lu; Li, Hai-mei; Li, Ze-hua; Yang, Li; Qian, Qiu-jin; Tang, Yi-lang; Cubells, Joseph F; Wang, Yu-feng.
Am J Med Genet B Neuropsychiatr Genet
; 156B(6): 730-6, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21761554
Polymorphisms of dopamine-beta-hydroxylase in ADHD children.
Lack of significant association between -1021C-->T polymorphism in the dopamine beta hydroxylase gene and attention deficit hyperactivity disorder.
A single nucleotide polymorphism at DBH, possibly associated with attention-deficit/hyperactivity disorder, associates with lower plasma dopamine beta-hydroxylase activity and is in linkage disequilibrium with two putative functional single nucleotide polymorphisms.
Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India.
The -1021 C/T DBH polymorphism is associated with neuropsychological performance among children and adolescents with ADHD.
[Association of dopamine beta-hydroxylase polymorphism with attention deficit hyperactivity disorder in children].
Association analyses of MAOA in Chinese Han subjects with attention-deficit/hyperactivity disorder: family-based association test, case-control study, and quantitative traits of impulsivity.
Polymorphisms and low plasma activity of dopamine-beta-hydroxylase in ADHD children.
Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorder.
Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.