Blame it on the Inputs: Overexcited Entorhinal Inputs Drive Dentate Gyrus Hyperexcitability in a Mouse Model of Dravet Syndrome
Author:
Affiliation:
1. Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA
Abstract
Funder
National Institute of Neurological Disorders and Stroke
Publisher
SAGE Publications
Subject
Neurology (clinical)
Link
http://journals.sagepub.com/doi/pdf/10.1177/15357597221112801
Reference10 articles.
1. Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy
2. Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome
3. De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
4. Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome
5. A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients
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