Differential Functional Changes of Nav1.2 Channel Causing SCN2A-Related Epilepsy and Status Epilepticus During Slow Sleep

Background: Nav1.2 encoded by the SCN2A gene is a brain-expressed voltage-gated sodium channel known to be associated with neurodevelopment disorders ranging from benign familial neonatal infantile seizures (BFIS) to developmental and epileptic encephalopathy (DEE) and autism spectrum disorder. Inte...

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Detalles Bibliográficos
Autores principales: Miao, Pu, Tang, Siyang, Ye, Jia, Tang, Jihong, Wang, Jianda, Zheng, Chaoguang, Li, Yuezhou, Feng, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170409/
https://www.ncbi.nlm.nih.gov/pubmed/34093402
http://dx.doi.org/10.3389/fneur.2021.653517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170409/
https://www.ncbi.nlm.nih.gov/pubmed/34093402
http://dx.doi.org/10.3389/fneur.2021.653517

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