Mesial temporal sclerosis in children with SCN1A mutation

J Child Neurol. 2013 Apr;28(4):541. doi: 10.1177/0883073812473365.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Epilepsy, Temporal Lobe / genetics*
  • Female
  • Humans
  • Male
  • Mutation / genetics*
  • NAV1.1 Voltage-Gated Sodium Channel / genetics*
  • Sclerosis / genetics*
  • Sclerosis / pathology*
  • Temporal Lobe / pathology*

Substances

  • NAV1.1 Voltage-Gated Sodium Channel