An 18-year-old man with dominant optic atrophy (DOA). The fundus
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Colour fundus and OCT findings in DOA. The images were obtained
Hereditary Optic Neuropathies
Genes, Free Full-Text
An 18-year-old man with dominant optic atrophy (DOA). The fundus
Hereditary optic neuropathies
A Missense Mutation in OPA1 Causes Dominant Optic Atrophy in a
Leber's Hereditary Optic Neuropathy – Case-Based Neuro-Ophthalmology
Ophthalmological description of a DOA patient. Results from
Dominant Optic Atrophy: for patients - Gene Vision
Optic Atrophy 1 disease: Malacards - Research Articles, Drugs
Genetic disorders affecting the optic nerve - ScienceDirect
A novel mutation located in the intermembrane space domain of
Genetic disorders affecting the optic nerve - ScienceDirect
Dominant optic atrophy: Culprit mitochondria in the optic nerve
2020–2021 BCSC Basic and Clinical Science Course™
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