| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10309839 | Seizure | 2012 | 5 Pages |
Abstract
The frequency of Myoclonin1/EFHC1 mutations in our sample is 7.3%. Thus, we conclude that mutations in the Myoclonin1/EFHC1 gene are an important cause of JME in Mexican patients.
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Authors
Aurelio Jara-Prado, Iris E. MartÃnez-Juárez, Adriana Ochoa, VÃctor M. González, MarÃa del Carmen Fernández-González-Aragón, Minerva López-Ruiz, Marco T. Medina, Julia N. Bailey, Antonio V. Delgado-Escueta, MarÃa Elisa Alonso,