(Q46696105)

24 December 2017

title

A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder (English)

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24 December 2017

attention deficit hyperactivity disorder

main subject

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1 reference

2

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24 December 2017

Ingeborg Winge

5

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24 December 2017

Jan Haavik

7

object named as

J Haavik

1 reference

24 December 2017

J McKinney

1

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24 December 2017

A Halmøy

3

1 reference

24 December 2017

M Dramsdahl

4

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24 December 2017

P M Knappskog

6

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24 December 2017

language of work or name

English

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publication date

1 April 2008

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24 December 2017

published in

Molecular Psychiatry

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24 December 2017

volume

13

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24 December 2017

issue

4

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24 December 2017

page(s)

365-367

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24 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.mp.4002152

exact match

0 references

cites work

Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

Association of functional polymorphisms of the human tryptophan hydroxylase 2 gene with risk for bipolar disorder in Han Chinese

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

Characterization of wild-type and mutant forms of human tryptophan hydroxylase 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

Partial characterization and three-dimensional-structural localization of eight mutations in exon 7 of the human phenylalanine hydroxylase gene associated with phenylketonuria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002152

21 January 2018

Identifiers

DOI

10.1038/SJ.MP.4002152

1 reference

24 December 2017

1 reference

24 December 2017