Concise Review: Stem Cell Models of SCN1A-Related Encephalopathies—Current Perspective and Future Therapies

Mutations in the SCN1A gene can cause a variety of phenotypes, ranging from mild forms, such as febrile seizures and generalized epilepsy with febrile seizures plus, to severe, such as Dravet and non-Dravet developmental epileptic encephalopathies. Until now, more than two thousand pathogenic varian...

Descripción completa

Detalles Bibliográficos
Autores principales: Zayat, Valery, Szlendak, Roza, Hoffman-Zacharska, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561991/
https://www.ncbi.nlm.nih.gov/pubmed/36231081
http://dx.doi.org/10.3390/cells11193119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561991/
https://www.ncbi.nlm.nih.gov/pubmed/36231081
http://dx.doi.org/10.3390/cells11193119

Ejemplares similares