De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy. - Stringer, Robin N.; Jurkovicova-Tarabova, Bohumila; Souza, Ivana A.; Ibrahim, Judy; Vacik, Tomas; Fathalla, Waseem Mahmoud; Hertecant, Jozef; Zamponi, Gerald W.; Lacinova, Lubica; Weiss, Norbert (Molecular Brain, 2021)