Retinal DiseasesRetinal DegenerationRetinal DystrophiesMuscular DystrophiesLeber Congenital AmaurosisRetinitis PigmentosaMyotonic DystrophyElectroretinographyEye Proteinscis-trans-IsomerasesMuscular Dystrophy, DuchenneRetinaFundus OculiPedigreePhotoreceptor Cells, VertebrateCorneal Dystrophies, HereditaryEye Diseases, HereditaryGenes, RecessiveMuscular Dystrophy, AnimalRetinal Pigment EpitheliumPeripherinsPigment Epithelium of EyeMutationConsanguinityNight BlindnessGenetic Diseases, InbornBlindnessDNA Mutational AnalysisRetinal Rod Photoreceptor CellsFuchs' Endothelial DystrophyLipofuscinLaurence-Moon SyndromeGenetic LinkagePhotoreceptor CellsMacular DegenerationChromosome MappingRetinal Cone Photoreceptor CellsDiseasePhenotypeGenes, DominantUsher SyndromesDark AdaptationVisual AcuityFluorescein AngiographyMuscular Dystrophy, FacioscapulohumeralDystrophinTomography, Optical CoherenceRhodopsinMutation, MissenseBardet-Biedl SyndromeOphthalmoscopyMicrophthalmosExonsLod ScoreMolecular Sequence DataCyclic Nucleotide Phosphodiesterases, Type 6ExomeAlstrom SyndromeVision, OcularVisual FieldsSyndromeNerve Tissue ProteinsVisual Field TestsHaplotypesMuscular Dystrophy, Emery-DreifussKidney Diseases, CysticMice, Inbred mdxPolymorphism, Single-Stranded ConformationalVision DisordersRod OpsinsIntermediate Filament ProteinsRetinal VesselsCodon, NonsenseOptic Atrophy, Hereditary, LeberBase SequenceDisease Models, AnimalGenotypeHomozygoteOphthalmoscopesGenetic MarkersGenetic TestingChoroid DiseasesNeuroaxonal DystrophiesOptic Atrophies, HereditaryCarrier ProteinsHeterozygoteOptic Disk DrusenSarcoglycansATP-Binding Cassette TransportersAge of OnsetRats, Mutant StrainsAmino Acid SequenceRod Cell Outer SegmentProteinsFrameshift MutationHeteroduplex AnalysisIntellectual DisabilityAbnormalities, MultipleMice, Inbred C57BLMembrane Proteins