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