A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder
- 18 March 2008
- journal article
- Published by Springer Nature in Molecular Psychiatry
- Vol. 13 (4) , 365-367
- https://doi.org/10.1038/sj.mp.4002152
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorderHuman Molecular Genetics, 2007
- Association of Functional Polymorphisms of the Human Tryptophan Hydroxylase 2 Gene With Risk for Bipolar Disorder in Han ChineseArchives of General Psychiatry, 2007
- Characterization of wild‐type and mutant forms of human tryptophan hydroxylase 2Journal of Neurochemistry, 2006
- The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genesMolecular Psychiatry, 2006
- Haplotype-Based Linkage of Tryptophan Hydroxylase 2 to Suicide Attempt, Major Depression, and Cerebrospinal Fluid 5-Hydroxyindoleacetic Acid in 4 PopulationsArchives of General Psychiatry, 2005
- Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive–compulsive disorderInternational Journal of Neuropsychopharmacology, 2005
- Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major DepressionNeuron, 2005
- Partial characterization and three‐dimensional‐structural localization of eight mutations in exon 7 of the human phenylalanine hydroxylase gene associated with phenylketonuriaEuropean Journal of Biochemistry, 1998