Funder
Dravet Syndrome Foundation
Reference41 articles.
1. “De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy,”;Claes;Am. J. Hum. Genet.,2001
2. “The genetics of Dravet syndrome,”;Marini;Epilepsia,2011
3. “SCN1A mutation—beyond dravet syndrome: a systematic review and narrative synthesis,”;Ding;Front. Neurol.,2021
4. “Determinación de la epidemiología, el flujo de pacientes y el tratamiento del síndrome de Dravet en España,”;Gil-Nagel Rein;Rev Neurol,2019
5. “Dravet syndrome—the polish family's perspective study,”;Paprocka;J. Clin. Med.,2021