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A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder.
https://arctichealth.org/en/permalink/ahliterature87145
Source
Mol Psychiatry. 2008 Apr;13(4):365-7
Publication Type
Article
Date
Apr-2008
More detail
Author
McKinney J.
Johansson S.
Halmøy A.
Dramsdahl M.
Winge I.
Knappskog P M
Haavik J.
Source
Mol Psychiatry. 2008 Apr;13(4):365-7
Date
Apr-2008
Language
English
Publication Type
Article
Keywords
Arginine - genetics
Attention Deficit Disorder with Hyperactivity - genetics
Base Sequence
Cell Line, Transformed
Family Health
Female
Humans
Male
Mutation - genetics
Norway
Tryptophan - genetics
Tryptophan Hydroxylase - genetics - metabolism
PubMed ID
18347598
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