Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome
Dravet syndrome (DS) is a neurodevelopmental disorder due to pathogenic variants in SCN1A encoding the Nav1.1 sodium channel subunit, characterized by treatment-resistant epilepsy, temperature-sensitive seizures, developmental delay/intellectual disability with features of autism spectrum disorder,...
Main Authors: | Joanna Mattis, Ala Somarowthu, Kevin M Goff, Evan Jiang, Jina Yom, Nathaniel Sotuyo, Laura M Mcgarry, Huijie Feng, Keisuke Kaneko, Ethan M Goldberg |
---|---|
Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2022-02-01
|
Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/69293 |
Similar Items
-
A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients
by: Yishan Sun, et al.
Published: (2016-07-01) -
Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations
by: Lucia Mora-Jimenez, et al.
Published: (2021-09-01) -
Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome
by: Kevin M Goff, et al.
Published: (2019-07-01) -
Patient with Dravet syndrome: A case report
by: Rukesh Yadav, et al.
Published: (2022-05-01) -
Compromised function in the Nav1.2 Dravet syndrome mutation R1312T
by: Christoph Lossin, et al.
Published: (2012-09-01)