Clinical Assessments and EEG Analyses of Encephalopathies Associated With Dynamin-1 Mutation

Epileptic encephalopathy, caused by mutations in the dynamin-1 (DNM1; NM_004408) gene, is a newly identified neurologic disorder in children. Thus far, the full clinical and electroencephalographic features of children with DNM1 mutation-related epileptic encephalopathy have not been established. Th...

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Bibliografiske detaljer

Principais autores:	Hua Li, Fang Fang, Manting Xu, Zhimei Liu, Ji Zhou, Xiaohui Wang, Xiaofei Wang, Tongli Han
Format:	Artigo
Sprog:	Inglês
Udgivet:	Frontiers Media S.A. 2019-12-01
Serier:	Frontiers in Pharmacology
Fag:	epileptic encephalopathy dynamin-1 mutation electroencephalogram, children
Online adgang:	https://www.frontiersin.org/article/10.3389/fphar.2019.01454/full
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