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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 

Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases.

The previously unrecognised association of myoclonus in two patients with LHON with the 11778/ND4 pathogenic mutation is described. EEG failed to disclose epileptic figures, and a back averaging study suggested that myoclonus was cortical in origin in both patients.[1]

References

  1. Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases. Carelli, V., Valentino, M.L., Liguori, R., Meletti, S., Vetrugno, R., Provini, F., Mancardi, G.L., Bandini, F., Baruzzi, A., Montagna, P. J. Neurol. Neurosurg. Psychiatr. (2001) [Pubmed]
 
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