Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome

Ann Neurol. 2012 Aug;72(2):298-300. doi: 10.1002/ana.23620.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Epilepsy, Benign Neonatal / diagnosis*
  • Epilepsy, Benign Neonatal / genetics*
  • Female
  • Humans
  • KCNQ2 Potassium Channel / genetics*
  • Male
  • Mutation / genetics*
  • Phenotype*

Substances

  • KCNQ2 Potassium Channel