Retinal DystrophiesMuscular DystrophiesRetinal DegenerationMyotonic DystrophyLeber Congenital AmaurosisMuscular Dystrophy, DuchenneMutation, MissenseRetinitis PigmentosaPoint MutationMutationCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesPedigreeEye ProteinsMuscular Dystrophy, AnimalFundus OculiGenes, RecessiveConsanguinityFrameshift MutationDNA Mutational AnalysisFuchs' Endothelial DystrophyRetinal DiseasesLaurence-Moon SyndromeEye Diseases, HereditaryPhotoreceptor Cells, VertebrateRetinaPeripherinsBlindnessExonsDystrophinMuscular Dystrophy, FacioscapulohumeralGenes, DominantCodon, NonsensePhenotypeMicrophthalmosBardet-Biedl SyndromeHeterozygotePigment Epithelium of EyeNight BlindnessSyndromeBase SequenceMolecular Sequence DataPhotoreceptor CellsGerm-Line MutationPolymorphism, Single-Stranded ConformationalAlstrom SyndromeHomozygoteDark AdaptationVisual AcuityRetinal Pigment EpitheliumPolymerase Chain ReactionMuscular Dystrophy, Emery-DreifussOptic Atrophy, Hereditary, LeberChromosome MappingUsher SyndromesMice, Inbred mdxGenetic LinkageAmino Acid SubstitutionGenotypeRetinal Rod Photoreceptor CellsFluorescein AngiographyOptic Atrophies, HereditaryGenetic TestingAmino Acid SequenceExomeRetinal Cone Photoreceptor CellsMacular DegenerationNeuroaxonal DystrophiesChoroid DiseasesAge of OnsetSarcoglycansKidney Diseases, CysticHeteroduplex AnalysisOptic Disk DrusenRats, Mutant StrainsSequence Analysis, DNAMembrane ProteinsMutation RateAbnormalities, MultipleLipofuscinCarrier ProteinsVisual FieldsRhodopsinAllelesNerve Tissue ProteinsTomography, Optical CoherenceProteinsLod ScoreDystroglycansIntellectual DisabilityMuscular Dystrophy, OculopharyngealVisual Field TestsMuscle, SkeletalReflex Sympathetic DystrophyVitelliform Macular DystrophyIntermediate Filament ProteinsVision DisordersOphthalmoscopyATP-Binding Cassette Transporters