TY  - JOUR
AU  - Salazar Corral, Juan José
AU  - Satriano, Andrea
AU  - Matamoros, José A.
AU  - Fernández Albarral, José
AU  - García Martín, Elena Salobrar
AU  - López Cuenca, Inés
AU  - Hoz Montañana, María Rosa De
AU  - Sánchez-Puebla Fernández, Lidia
AU  - Ramírez Sebastián, José Manuel
AU  - Alonso, Cristina
AU  - Satta, Valentina
AU  - Hernández Fisac, Inés
AU  - Sagredo Ezquioga, Onintza
AU  - Ramírez Sebastián, Ana Isabel
DA  - Received: 19 December 2022 / Revised: 26 January 2023 / Accepted: 29 January 2023 / Published: 1 February 2023(This article belongs to the Special Issue Advanced Researches in Retina)
PY  - 2023
DO  - 10.3390/ijms24032727
SN  - 1422-0067
UR  - https://hdl.handle.net/20.500.14352/72989
T2  - International Journal of Molecular Sciences
AB  - 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...
LA  - eng
PB  - MDPI
KW  - Dravet syndrome
KW  - Retina
KW  - Astrocytes
KW  - Microglia
KW  - Retinal ganglion cells
KW  - GABAergic amacrine cells
KW  - Syn-Cre/Scn1aWT/A1783V mice
TI  - Retinal Tissue Shows Glial Changes in a Dravet Syndrome Knock-in Mouse Model
TY  - journal article
VL  - 24
ER  -