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...

Täydet tiedot

Bibliografiset tiedot

Päätekijät:	Valery Zayat, Roza Szlendak, Dorota Hoffman-Zacharska
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	MDPI AG 2022-10-01
Sarja:	Cells
Aiheet:	<i>SCN1A</i>-related disorders developmental and epileptic encephalopathies Nav1.1 functional studies stem cell models organoids
Linkit:	https://www.mdpi.com/2073-4409/11/19/3119
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