Novel K+ channel genes in benign familial neonatal convulsions

Epilepsia. 2000 Aug;41(8):1066-7. doi: 10.1111/j.1528-1157.2000.tb00301.x.
No abstract available

MeSH terms

  • Adolescent
  • Adult
  • Chromosomes, Human, Pair 20 / genetics
  • Chromosomes, Human, Pair 8 / genetics
  • DNA Mutational Analysis
  • Epilepsy, Benign Neonatal / genetics*
  • Frameshift Mutation
  • Genes, Dominant / genetics
  • Humans
  • Infant
  • Infant, Newborn
  • Mutation*
  • Mutation, Missense
  • Polymorphism, Single-Stranded Conformational
  • Potassium Channels / genetics*

Substances

  • Potassium Channels