Sexual dimorphism in epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene
Rogério R. Gerbatin, Joana Augusto, Halima Boutouil, Cristina Ruedell Reschke, David Clifford Henshall
This study investigates sex differences and long-term comorbidities in Scn1a(+/-)tm1Kea mice modeling Dravet Syndrome, finding sex-specific seizure patterns and reduced behavioral impairments in older mice.
bioRxiv · Aug 27, 2021 · PreprintNeuroscience