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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Frontiers Media S.A.,
2019-12-01T00:00:00Z.
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