A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder

Mol Psychiatry. 2008 Apr;13(4):365-7. doi: 10.1038/sj.mp.4002152.
No abstract available

Publication types

  • Letter

MeSH terms

  • 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*
  • Tryptophan Hydroxylase / metabolism

Substances

  • Tryptophan
  • Arginine
  • TPH2 protein, human
  • Tryptophan Hydroxylase