Lack of significant association between −1021C→T polymorphism in the dopamine beta hydroxylase gene and attention deficit hyperactivity disorder
- 1 July 2006
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 402 (1-2) , 12-16
- https://doi.org/10.1016/j.neulet.2006.03.036
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- The Nature and Heritability of Attention-Deficit/Hyperactivity DisorderPublished by Elsevier ,2018
- Haploview: analysis and visualization of LD and haplotype mapsBioinformatics, 2004
- Linkage disequilibrium analysis of the dopamine beta-hydroxylase gene in persistent attention deficit hyperactivity disorderPsychiatric Genetics, 2004
- Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these lociMolecular Psychiatry, 2003
- Mutations in the dopamine β‐hydroxylase gene are associated with human norepinephrine deficiencyAmerican Journal of Medical Genetics, 2002
- Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected childrenMolecular Psychiatry, 1999
- Dopamine β-hydroxylase: two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variationHuman Genetics, 1998
- Revision and Restandardization of the Conners Teacher Rating Scale (CTRS-R): Factor Structure, Reliability, and Criterion ValidityJournal of Abnormal Child Psychology, 1998
- Dopamine‐β‐hydroxylase deficiency in humansNeurology, 1990
- A simple salting out procedure for extracting DNA from human nucleated cellsNucleic Acids Research, 1988