Retinal DystrophiesMuscular DystrophiesRetinal DegenerationMyotonic DystrophyLeber Congenital AmaurosisMuscular Dystrophy, DuchenneRetinitis PigmentosaCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesPedigreeEye ProteinsMuscular Dystrophy, AnimalKidney Failure, ChronicFundus OculiGenes, RecessiveConsanguinityGenetic Diseases, InbornRetinal DiseasesMutationFuchs' Endothelial DystrophyLaurence-Moon SyndromeEye Diseases, HereditaryKidney DiseasesGenetic LinkageDNA Mutational AnalysisDiseaseRetinaPhotoreceptor Cells, VertebrateChromosome MappingPeripherinsBlindnessPhenotypeMuscular Dystrophy, FacioscapulohumeralGenes, DominantDystrophinBardet-Biedl SyndromeKidney Diseases, CysticPigment Epithelium of EyeRenal DialysisMicrophthalmosPhotoreceptor CellsNight BlindnessLod ScoreMutation, MissenseSyndromeExomeAlstrom SyndromeDark AdaptationVisual AcuityExonsRetinal Pigment EpitheliumHaplotypesMuscular Dystrophy, Emery-DreifussMacular DegenerationFluorescein AngiographyMice, Inbred mdxMolecular Sequence DataRetinal Rod Photoreceptor CellsCodon, NonsenseHomozygoteUsher SyndromesOptic Atrophy, Hereditary, LeberGenetic MarkersGenetic TestingAge of OnsetHeterozygoteGenotypeRetinal Cone Photoreceptor CellsChoroid DiseasesNeuroaxonal DystrophiesNerve Tissue ProteinsOptic Atrophies, HereditaryProteinuriaBase SequenceRats, Mutant StrainsOptic Disk DrusenSarcoglycansProteinsGlomerular Filtration RateKidneyLipofuscinDiabetic NephropathiesVisual FieldsFrameshift MutationDisease Models, AnimalPolymorphism, Single-Stranded ConformationalHeteroduplex AnalysisIntellectual DisabilityAbnormalities, MultipleGenetic Predisposition to DiseaseTomography, Optical CoherencePolymorphism, Single NucleotideCarrier ProteinsRhodopsinCreatinineMembrane ProteinsMuscular Dystrophy, OculopharyngealDystroglycansVisual Field Tests