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Tryptophan hydroxylase 2
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
(Redirected from TPH2)
 | This article is a stub. |
Tryptophan Hydroxylase 2 or neuronal tryptophan hydroxylase or TPH2 or ADHD7 is a gene found by Goertzel et al. (2006) to be associated with the development of chronic fatigue syndrome.[1][2]
Function[edit | edit source]
ME/CFS[edit | edit source]
Notable studies[edit | edit source]
- 2006, Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes[1] - (Full text)
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- ↑ Jump up to: 1.0 1.1 Goertzel, Benjamin N.; Pennachin, Cassio; de Souza Coelho, Lucio; Gurbaxani, Brian; Maloney, Elizabeth M.; Jones, James F. (April 2006). "Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome". Pharmacogenomics. 7 (3): 475–483. doi:10.2217/14622416.7.3.475. ISSN 1462-2416. PMID 16610957.
- ↑ "TPH2 Gene card". Gene cards. Retrieved March 18, 2022.
