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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 thousand pathogenic...

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Principais autores: Valery Zayat, Roza Szlendak, Dorota Hoffman-Zacharska
Format: Artigo
Sprog:Inglês
Udgivet: MDPI AG 2022-10-01
Serier:Cells
Fag:
<i>SCN1A</i>-related disorders
developmental and epileptic encephalopathies
Nav1.1
functional studies
stem cell models
organoids
Online adgang:https://www.mdpi.com/2073-4409/11/19/3119
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