KCNQ2 gene mutations and neonatal epilepsy

Med Clin (Barc). 2021 Dec 24;157(12):589-590. doi: 10.1016/j.medcli.2021.01.019. Epub 2021 May 4.
[Article in English, Spanish]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Epilepsy* / genetics
  • Humans
  • Infant, Newborn
  • KCNQ2 Potassium Channel / genetics
  • Mutation

Substances

  • KCNQ2 Potassium Channel
  • KCNQ2 protein, human