Nodular heterotopia: a rare finding in patients with epilepsy and SCN1A mutation

Arq Neuropsiquiatr. 2021 Oct;79(10):936-937. doi: 10.1590/0004-282X-ANP-2021-0084.
No abstract available

MeSH terms

  • Epilepsy* / genetics
  • Humans
  • Mutation
  • NAV1.1 Voltage-Gated Sodium Channel / genetics

Substances

  • NAV1.1 Voltage-Gated Sodium Channel
  • SCN1A protein, human