Dravet syndrome (DS) is characterized by severe infant-onset myoclonic epilepsy along with delayed psychomotor development and heightened premature mortality. A primary monogenic cause is mutation of the SCN1A gene. which encodes the voltage-gated sodium channel subunit Nav1. 1. https://www.sukrensi.com/flash-offer-ILOOTPAPERIE-Washi-Tape-best-find/