[Non-dystrophic myotonias. Diagnostic approach in a case related with a mutation in the sodium-channel gene]

Rev Neurol. 2010 Nov 1;51(9):571-2.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Humans
  • Male
  • Mutation*
  • Myotonic Disorders / congenital
  • Myotonic Disorders / diagnosis*
  • Myotonic Disorders / genetics*
  • NAV1.4 Voltage-Gated Sodium Channel
  • Sodium Channels / genetics*
  • Syndrome

Substances

  • NAV1.4 Voltage-Gated Sodium Channel
  • SCN4A protein, human
  • Sodium Channels