Tryptophan hydroxylase 2

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history

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]

  1. 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.
  2. "TPH2 Gene card". Gene cards. Retrieved March 18, 2022.