A novel NTRK1 mutation in a patient with congenital insensitivity to pain with anhidrosis

Acta Neurol Belg. 2015 Sep;115(3):509-11. doi: 10.1007/s13760-014-0405-9. Epub 2014 Dec 18.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Child
  • Hereditary Sensory and Autonomic Neuropathies / genetics*
  • Humans
  • Male
  • Mutation
  • Pedigree
  • Receptor, trkA / genetics*

Substances

  • Receptor, trkA