An 18-year-old man with dominant optic atrophy (DOA). The fundus
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Genes, Free Full-Text
A novel mutation located in the intermembrane space domain of
Characterization of SSBP1-related optic atrophy and foveopathy
An 18-year-old man with dominant optic atrophy (DOA). The fundus
IJMS, Free Full-Text
Genes, Free Full-Text
Dominant Optic Atrophy: A Teenager with Progressive Painless
2020–2021 BCSC Basic and Clinical Science Course™
Stresses, Free Full-Text
Genetic disorders affecting the optic nerve - ScienceDirect
First submicroscopic inversion of the OPA1 gene identified in
Hereditary Optic Neuropathies
Optic Nerve Diseases that may Masquerade as Macular Diseases
Young patient with long-standing reduced vision
