sodium channel protein type 8 subunit alpha isoform X1 [Mus musculus]

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Cardiac-Specific Deletion of Scn8a Mitigates Dravet Syndrome-Associated Sudden Death in Adults. [JACC Clin Electrophysiol. 2024]
Cardiac-Specific Deletion of Scn8a Mitigates Dravet Syndrome-Associated Sudden Death in Adults.
King DR, Demirtas M, Tarasov M, Struckman HL, Meng X, Nassal D, Moise N, Miller A, Min D, Soltisz AM, et al. JACC Clin Electrophysiol. 2024 May; 10(5):829-842. Epub 2024 Feb 28.
Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia. [EBioMedicine. 2023]
Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia.
Lyu H, Boßelmann CM, Johannesen KM, Koko M, Ortigoza-Escobar JD, Aguilera-Albesa S, Garcia-Navas Núñez D, Linnankivi T, Gaily E, van Ruiten HJA, et al. EBioMedicine. 2023 Dec; 98:104855. Epub 2023 Oct 28.
Social Deficits and Cerebellar Degeneration in Purkinje Cell Scn8a Knockout Mice. [Front Mol Neurosci. 2022]
Social Deficits and Cerebellar Degeneration in Purkinje Cell Scn8a Knockout Mice.
Yang X, Yin H, Wang X, Sun Y, Bian X, Zhang G, Li A, Cao A, Li B, Ebrahimi-Fakhari D, et al. Front Mol Neurosci. 2022; 15:822129. Epub 2022 Apr 26.

RefSeq mRNA
See reference mRNA sequence for the Scn8a gene (XM_017316514.2).
RefSeq protein isoforms
See 12 reference sequence protein isoforms for the Scn8a gene.

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