Association of rs2129575 in the tryptophan hydroxylase 2 gene with clinical phenotypes of autism spectrum disorders

Psychiatry Clin Neurosci. 2013 Sep;67(6):457-8. doi: 10.1111/pcn.12080.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Alleles
  • Child Development Disorders, Pervasive / epidemiology
  • Child Development Disorders, Pervasive / genetics*
  • Child Development Disorders, Pervasive / psychology*
  • Diagnostic and Statistical Manual of Mental Disorders
  • Female
  • Humans
  • Intelligence Tests
  • Japan / epidemiology
  • Male
  • Neuropsychological Tests
  • Phenotype
  • Tryptophan Hydroxylase / genetics*

Substances

  • TPH2 protein, human
  • Tryptophan Hydroxylase