Retinal Tissue Shows Glial Changes in a Dravet Syndrome Knock-in Mouse Model

Dravet syndrome (DS) is an epileptic encephalopathy caused by mutations in the Scn1a gene encoding the α1 subunit of the Nav1.1 sodium channel, which is associated with recurrent and generalized seizures, even leading to death. In experimental models of DS, histological alterations have been found i...

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Detalles Bibliográficos
Autores principales: Salazar, Juan J., Satriano, Andrea, Matamoros, José A., Fernández-Albarral, José A., Salobrar-García, Elena, López-Cuenca, Inés, de Hoz, Rosa, Sánchez-Puebla, Lidia, Ramírez, José M., Alonso, Cristina, Satta, Valentina, Hernández-Fisac, Inés, Sagredo, Onintza, Ramírez, Ana I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9916888/
https://www.ncbi.nlm.nih.gov/pubmed/36769051
http://dx.doi.org/10.3390/ijms24032727

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9916888/
https://www.ncbi.nlm.nih.gov/pubmed/36769051
http://dx.doi.org/10.3390/ijms24032727

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