Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)106-108
Number of pages3
JournalSeizure
Volume65
DOIs
Publication statusPublished - Feb 1 2019

Keywords

  • Genetic ataxia
  • KCNA2 gene
  • Potassium channelopathy
  • Progressive myoclonus epilepsy

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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