1. Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsy 
Aurelio Jara-Prado, Iris E. Martínez-Juárez, Adriana Ochoa, Víctor M. González, María del Carmen Fernández-González-Aragón, Minerva López-Ruiz, Marco T. Medina, Julia N. Bailey, Antonio V. Delgado-Escueta, María Elisa Alonso 
Seizure - European Journal of Epilepsy 
Volume 21, Issue 7, Pages (September 2012)
DOI: /j.seizure
Copyright © 2012 British Epilepsy Association Terms and Conditions

2. Fig. 1
Families with novel EFHC1 mutations. Brief description: Circles: female; Square: male; Circles and square filled: affected subjects; Circles and square empty: non affected subjects; M: mutated; N: no mutated. *Normal EEG. **Abnormal EEG.
Seizure - European Journal of Epilepsy  , DOI: ( /j.seizure )
Copyright © 2012 British Epilepsy Association Terms and Conditions

3. Fig. 2
Seizure - European Journal of Epilepsy  , DOI: ( /j.seizure )
Copyright © 2012 British Epilepsy Association Terms and Conditions

4. Fig. 3
Diagram of genomic organization of the EFHC1 gene. New mutations are shown in bold type.
Seizure - European Journal of Epilepsy  , DOI: ( /j.seizure )
Copyright © 2012 British Epilepsy Association Terms and Conditions