Optic AtrophyOptic Atrophy, Autosomal DominantAtrophyOptic Atrophies, HereditaryOptic NerveMuscular AtrophyWolfram SyndromeOptic DiskGTP PhosphohydrolasesOptic Atrophy, Hereditary, LeberMuscular Atrophy, SpinalOptic NeuritisHereditary Sensory and Motor NeuropathyMultiple System AtrophyOptic ChiasmRetinal Ganglion CellsSpinal Muscular Atrophies of ChildhoodPedigreePapilledemaOptic Nerve InjuriesVision DisordersVisual AcuityOlivopontocerebellar AtrophiesDNA, MitochondrialBlindnessGyrate AtrophyEye DiseasesRetinaOnchocerciasis, OcularMagnetic Resonance ImagingOptic Neuropathy, IschemicOptic Lobe, NonmammalianGenes, RecessiveGlutaratesGeographic AtrophyCerebellar AtaxiaOptic FlowMitochondrial DiseasesSyndromeMyoclonic Cerebellar DyssynergiaDiabetes InsipidusMitochondrial DynamicsVision, LowMitochondrial ProteinsMutationElectroretinographyFundus OculiMicrocephalyNerve FibersVisual FieldsSurvival of Motor Neuron 1 ProteinOptics and PhotonicsMutation, MissenseColor Vision DefectsMuscular Disorders, AtrophicMitochondriaDNA Mutational AnalysisEvoked Potentials, VisualOptic Nerve GliomaSMN Complex ProteinsOptic Nerve DiseasesCodon, NonsenseConsanguinityGenetic HeterogeneityRetinal DiseasesNADH DehydrogenaseDisease Models, AnimalLeigh DiseaseVisual Field TestsNeurodegenerative DiseasesSurvival of Motor Neuron 2 ProteinGenes, DominantDeafnessHindlimb SuspensionPhenotypeBrainGenetic LinkageHearing Loss, SensorineuralChromosomes, Human, Pair 3Founder EffectIntellectual DisabilityMuscle, SkeletalMembrane ProteinsBulbo-Spinal Atrophy, X-LinkedAbnormalities, MultipleTomography, Optical CoherenceHomozygoteOphthalmoscopyOptic Disk Drusen