Multiomic Analyses Reveal Brainstem Metabolic Changes in a Mouse Model of Dravet Syndrome

Dravet Syndrome (DS) is a severe genetic epileptic encephalopathy caused by mutations in the <i>SCN1A</i> gene that encodes the voltage-gated sodium channel (Na_V1.1) subunit alpha. DS is characterized by intractable seizures, progressive developmental delay, cognitive impairment, and high...

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Autors principals:	Ashwini Sri Hari, Alexandria M. Chan, Audrey Scholl, Aidan Mulligan, Janint Camacho, Ireland Rose Kearns, Gustavo Vasquez Opazo, Jenna Cheminant, Teresa Musci, Min-Jee Goh, Alessandro Venosa, Philip J. Moos, Martin Golkowski, Cameron S. Metcalf
Format:	Artigo
Idioma:	Inglês
Publicat:	MDPI AG 2025-12-01
Col·lecció:	Cells
Matèries:	Dravet Syndrome sudden unexpected death in epilepsy (SUDEP) brainstem metabolism
Accés en línia:	https://www.mdpi.com/2073-4409/15/1/67
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