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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Main Authors: Hua Li (Author), Fang Fang (Author), Manting Xu (Author), Zhimei Liu (Author), Ji Zhou (Author), Xiaohui Wang (Author), Xiaofei Wang (Author), Tongli Han (Author)
Format: Book
Published: Frontiers Media S.A., 2019-12-01T00:00:00Z.
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