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

Mutations in the <i>SCN1A</i> 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 thousan...

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Bibliographic Details
Main Authors: Valery Zayat, Roza Szlendak, Dorota Hoffman-Zacharska
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/19/3119

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