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,...

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Detalles Bibliográficos
Autores principales: Mattis, Joanna, Somarowthu, Ala, Goff, Kevin M, Jiang, Evan, Yom, Jina, Sotuyo, Nathaniel, Mcgarry, Laura M, Feng, Huijie, Kaneko, Keisuke, Goldberg, Ethan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Genetics and Genomics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920506/
https://www.ncbi.nlm.nih.gov/pubmed/35212623
http://dx.doi.org/10.7554/eLife.69293

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920506/
https://www.ncbi.nlm.nih.gov/pubmed/35212623
http://dx.doi.org/10.7554/eLife.69293

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