Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome

Dravet syndrome is a severe developmental and epileptic encephalopathy mostly caused by heterozygous mutation of the SCN1A gene encoding the voltage-gated sodium channel α subunit Na(v)1.1. Multiple seizure types, cognitive deterioration, behavioral disturbances, ataxia, and sudden unexpected death...

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Detalles Bibliográficos
Autores principales: Lersch, Robert, Jannadi, Rawan, Grosse, Leonie, Wagner, Matias, Schneider, Marius Frederik, von Stülpnagel, Celina, Heinen, Florian, Potschka, Heidrun, Borggraefe, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623613/
https://www.ncbi.nlm.nih.gov/pubmed/35414300
http://dx.doi.org/10.1177/10738584221088244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623613/
https://www.ncbi.nlm.nih.gov/pubmed/35414300
http://dx.doi.org/10.1177/10738584221088244

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