However, these data are in accordance with other DS models that were reported to have normal rotarod performance, including models with deletions in the Scn1a gene (Niibori et al., 2020; Patra et al., 2020; Valassina et al., 2022) or mice harboring the Scn1a R1407X nonsense mutation (Ito et al., 2013). The gene discussed is SCN1A; the disease is Dravet syndrome.