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...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2020-01-01
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| Series: | Epilepsy & Behavior Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S258998641930053X |