Dravet Syndrome (DS) is most often caused by heterozygous loss-of-function mutations in the voltage-gated sodium channel gene SCN1A (Nav1. 1). resulting in severe epilepsy and neurodevelopmental impairment thought to be cause by reduced interneuron excitability. However. https://www.nacrack.com/hot-find-892-Renegade-8-great-pick/