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Published byHeloïse Cormier Modified over 6 years ago
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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
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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
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Fig. 2 Seizure - European Journal of Epilepsy , DOI: ( /j.seizure ) Copyright © 2012 British Epilepsy Association Terms and Conditions
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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
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