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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Detalles Bibliográficos
Autores principales: Li, Hua, Fang, Fang, Xu, Manting, Liu, Zhimei, Zhou, Ji, Wang, Xiaohui, Wang, Xiaofei, Han, Tongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Pharmacology
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

Internet

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

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