SCN8A encephalopathy: Mechanisms and models
Author:
Affiliation:
1. Department of Human GeneticsUniversity of Michigan Ann Arbor Michigan
Funder
Dravet Syndrome Foundation
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/epi.14703
Reference29 articles.
1. Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’
2. Mutation Detection in the and Alleles of the Sodium Channel
3. A Missense Mutation in the Sodium Channel Scn8a Is Responsible for Cerebellar Ataxia in the Mouse Mutantjolting
4. De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP
5. Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy
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