Mutations in KCNT1 cause a spectrum of focal epilepsies

Rikke S. Moller, Sarah E. Heron, Line H. G. Larsen, Chiao Xin Lim, Michael G. Ricos, Marta A. Bayly, Marjan J. A. van Kempen, Sylvia Klinkenberg, Ian Andrews, Kent Kelley, Gabriel M. Ronen, David Callen, Jacinta M. McMahon, Simone C. Yendle, Gemma L. Carvill, Heather C. Mefford, Rima Nabbout, Annapurna Poduri, Pasquale Striano, Maria G. BagliettoFederico Zara, Nicholas J. Smith, Clair Pridmore, Elena Gardella, Marina Nikanorova, Hans Atli Dahl, Pia Gellert, Ingrid E. Scheffer, Boudewijn Gunning, Bente Kragh-Olsen, Leanne M. Dibbens

Research output: Contribution to journalArticleAcademicpeer-review

24 Citations (Scopus)
Original languageEnglish
Pages (from-to)E114-E120
JournalEpilepsia
Volume56
Issue number9
DOIs
Publication statusPublished - Sep 2015

Keywords

  • KCNT1
  • Autosomal dominant nocturnal frontal lobe epilepsy
  • Epileptic encephalopathy
  • Cardiac arrhythmia
  • Sudden unexpected death in epilepsy

Cite this

Moller, R. S., Heron, S. E., Larsen, L. H. G., Lim, C. X., Ricos, M. G., Bayly, M. A., van Kempen, M. J. A., Klinkenberg, S., Andrews, I., Kelley, K., Ronen, G. M., Callen, D., McMahon, J. M., Yendle, S. C., Carvill, G. L., Mefford, H. C., Nabbout, R., Poduri, A., Striano, P., ... Dibbens, L. M. (2015). Mutations in KCNT1 cause a spectrum of focal epilepsies. Epilepsia, 56(9), E114-E120. https://doi.org/10.1111/epi.13071