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Mitochondrial Translation Optimizer-1 Mutation as a Cause of Hereditary Optic Neuropathy | Emily Li; Francine Testa; Valentina Emmanuele; Christiane De Araujo; Martins Moreno; Michio Hirano; Robert Lesser | Mitochondrial translation optimizer-1 (MTO1) mutations are a rare cause of hereditary optic neuropathy, with fewer than ten affected families reported in literature. Of these, only one family was reported to have vision loss. We present a case of hereditary optic neuropathy secondary to a mutation i... | 20180304_nanos_posters_025 |