Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsy
Seizure - European Journal of Epilepsy, 06/26/2012
Jara–Prado A et al. – The frequency of Myoclonin1/EFHC1 mutations in the sample is 7.3%. Thus, the authors conclude that mutations in the Myoclonin1/EFHC1 gene are an important cause of juvenile myoclonic epilepsy (JME) in Mexican patients.