A Rare ND5 Mutation Causing Leber's Hereditary Optic Neuropathy.

Bhadra U Pandya1, Amir R Vosoughi2, Aaditeya Jhaveri1

  • 1Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Summary

This case report details a rare ND5 gene mutation (m.13528A>G) causing Leber's hereditary optic neuropathy (LHON). The study expands understanding of this mutation's clinical presentation and patient outcomes.

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