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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915043/ https://www.ncbi.nlm.nih.gov/pubmed/31920647 http://dx.doi.org/10.3389/fphar.2019.01454 |