Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy

Neurology. 2014 Nov 18;83(21):1991. doi: 10.1212/WNL.0000000000001041.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Female
  • Hereditary Sensory and Autonomic Neuropathies / genetics*
  • Hereditary Sensory and Autonomic Neuropathies / pathology*
  • Humans
  • Male
  • Mutation*
  • Phenotype*
  • TRPV Cation Channels / genetics*

Substances

  • TRPV Cation Channels