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Articles of Interest

• La Morgia, C., Achilli, A., Iommarini, L., Barboni, P., Pala, M., Olivieri, A., Zanna, C., Vidoni, S., Tonon, C., Lodi, R. and Vetrugno, R. (2008). Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. Neurology, 70(10), 762-770.
• Zsurka, G., Hampel, K.G., Nelson, I., Jardel, C., Mirandola, S.R., Sassen, R., Kornblum, C., Marcorelles, P., Lavoué, S., Lombès, A. and Kunz, W.S. (2010). Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNAPhe gene. Neurology, 74(6), 507-512.
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