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Juvenile myoclonic epilepsy mimic associated with CHD2 gene mutation
This paper reports the electroclinical manifestations of an epilepsy syndrome associated with a chromodomain helicase DNA-binding protein 2 (CHD2) gene mutation with clinical semiology and electroencephalographic (EEG) features consistent with juvenile myoclonic epilepsy (JME). Myoclonic and myoclon...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976925/ https://www.ncbi.nlm.nih.gov/pubmed/31993582 http://dx.doi.org/10.1016/j.ebr.2019.100355 |