A novel KCNQ3 gene mutation in a child with infantile convulsions and partial epilepsy with centrotemporal spikes

Eur J Paediatr Neurol. 2015 Jan;19(1):102-3. doi: 10.1016/j.ejpn.2014.08.006. Epub 2014 Sep 18.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Epilepsy / genetics*
  • Epilepsy, Rolandic / genetics*
  • Epilepsy, Rolandic / physiopathology
  • Female
  • Humans
  • Infant
  • KCNQ3 Potassium Channel / genetics*
  • Mutation / genetics*
  • Seizures / genetics*

Substances

  • KCNQ3 Potassium Channel
  • KCNQ3 protein, human