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TitleCreatorDescriptionIdentifier
1 Mitochondrial Translation Optimizer-1 Mutation as a Cause of Hereditary Optic NeuropathyEmily Li, Francine Testa, Valentina Emmanuele, Christiane De Araujo Martins Moreno, Michio Hirano, Robert LesserMitochondrial 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
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