Whole-exome sequencing of patients with juvenile myoclonic epilepsy
Background. Juvenile myoclonic epilepsy (JME) is the most common type of idiopathic generalized epilepsy with onset in adolescence and adulthood. During medical genetic counseling in probands with JME, aggravated epilepsy-related heredity is often detected. However, specific genetic variants of JME...
| Main Authors: | , , , , , , |
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| 格式: | Article |
| 語言: | Russian |
| 出版: |
IRBIS LLC
2022-10-01
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| 叢編: | Эпилепсия и пароксизмальные состояния |
| 主題: | |
| 在線閱讀: | https://www.epilepsia.su/jour/article/view/821 |