Do All Roads Lead to Rome? Genes Causing Dravet Syndrome and Dravet Syndrome-Like Phenotypes

BACKGROUND: Dravet syndrome (DS) is a severe epileptic encephalopathy mainly caused by haploinsufficiency of the gene SCN1A, which encodes the voltage-gated sodium channel Na(V)1. 1 in the brain. While SCN1A mutations are known to be the primary cause of DS, other genes that may cause DS are poorly...

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Detalles Bibliográficos
Autores principales: Ding, Jiangwei, Wang, Lei, Jin, Zhe, Qiang, Yuanyuan, Li, Wenchao, Wang, Yangyang, Zhu, Changliang, Jiang, Shucai, Xiao, Lifei, Hao, Xiaoyan, Hu, Xulei, Li, Xinxiao, Wang, Feng, Sun, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961694/
https://www.ncbi.nlm.nih.gov/pubmed/35359639
http://dx.doi.org/10.3389/fneur.2022.832380

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961694/
https://www.ncbi.nlm.nih.gov/pubmed/35359639
http://dx.doi.org/10.3389/fneur.2022.832380

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