TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome-Reference-Cited by-同舟云学术

TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome

Published:2011-03-18 Issue:5 Volume:52 Page:580-587
ISSN:0021-9630
Container-title:Journal of Child Psychology and Psychiatry
language:en
Short-container-title:

Author:

Dykens Elisabeth M.,Roof Elizabeth,Bittel Douglas,Butler Merlin G.

Publisher

Wiley

Subject

Psychiatry and Mental health,Developmental and Educational Psychology,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-7610.2011.02365.x/fullpdf

Reference42 articles.

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2. A regulatory variant of the human tryptophan hydroxylase-2 gene biases amydala reactivity;Brown;Molecular Psychiatry,2005

3. Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome;Butler;American Journal of Medical Genetics,2007

4. Amydala responsiveness is modulated by tryptophan hydroxylase-2 gene variation;Canli;Journal of Neural Transmission,2005

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