Retinal DystrophiesMuscular DystrophiesRetinal DegenerationMyotonic DystrophyLeber Congenital AmaurosisMuscular Dystrophy, DuchenneRetinitis PigmentosaCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesPedigreeEye ProteinsMuscular Dystrophy, AnimalFundus OculiGenes, RecessiveConsanguinityGenetic Diseases, InbornRetinal DiseasesFuchs' Endothelial DystrophyMutationLaurence-Moon SyndromeEye Diseases, HereditaryDNA Mutational AnalysisDiseaseRetinaGenetic LinkagePhotoreceptor Cells, VertebratePeripherinsChromosome MappingBlindnessMuscular Dystrophy, FacioscapulohumeralGenes, DominantDystrophinPhenotypePigment Epithelium of EyeBardet-Biedl SyndromeMicrophthalmosPhotoreceptor CellsNight BlindnessLod ScoreMutation, MissenseExomeAlstrom SyndromeDark AdaptationSyndromeVisual AcuityRetinal Pigment EpitheliumExonsHaplotypesMuscular Dystrophy, Emery-DreifussMacular DegenerationKidney Diseases, CysticFluorescein AngiographyMice, Inbred mdxRetinal Rod Photoreceptor CellsMolecular Sequence DataCodon, NonsenseUsher SyndromesOptic Atrophy, Hereditary, LeberHomozygoteRetinal Cone Photoreceptor CellsGenetic MarkersGenetic TestingChoroid DiseasesNeuroaxonal DystrophiesNerve Tissue ProteinsOptic Atrophies, HereditaryHeterozygoteOptic Disk DrusenSarcoglycansAge of OnsetBase SequenceLipofuscinRats, Mutant StrainsGenotypeVisual FieldsProteinsFrameshift MutationPolymorphism, Single-Stranded ConformationalHeteroduplex AnalysisIntellectual DisabilityAbnormalities, MultipleTomography, Optical CoherenceRhodopsinCarrier ProteinsMuscular Dystrophy, OculopharyngealDystroglycansVisual Field TestsReflex Sympathetic DystrophyDatabases, GeneticChromosomes, Human, Pair 4Genetic Predisposition to DiseasePolymorphism, Single NucleotideGenome, HumanMembrane ProteinsAmino Acid SequenceVision DisordersHepatolenticular DegenerationUtrophinOphthalmoscopy