Genotype-phenotype association in patients with SCN4A mutation - Authors' reply

Lancet. 2019 Jun 8;393(10188):2301-2302. doi: 10.1016/S0140-6736(19)30214-4. Epub 2019 Jun 6.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Genetic Association Studies
  • Humans
  • Mutation
  • NAV1.4 Voltage-Gated Sodium Channel / genetics*

Substances

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