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Updated: Mar 7, 2026

A Behavioral Screen for Heat-Induced Seizures in Mouse Models of Epilepsy
Published on: July 12, 2021
SCN3A deficiency associated with increased seizure susceptibility
Tyra Lamar1, Carlos G Vanoye2, Jeffrey Calhoun2
1Department of Human Genetics, Emory University, Atlanta, GA, USA.
Loss-of-function mutations in the SCN3A gene, which codes for the Nav1.3 sodium channel, can increase epilepsy risk. This study identifies a new SCN3A variant and shows reduced Nav1.3 channel activity contributes to seizures.
Area of Science:
- Neuroscience
- Genetics
- Molecular Biology
Background:
- Mutations in brain sodium channel genes (SCN1A, SCN2A, SCN3A, SCN8A) are linked to epilepsy.
- SCN3A gene mutations, specifically affecting the Nav1.3 alpha subunit, are found in focal epilepsy patients.
- Both gain- and loss-of-function SCN3A mutations may increase seizure susceptibility.
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