Retinal DystrophiesMuscular DystrophiesRetinal DegenerationMyotonic DystrophyPedigreeLeber Congenital AmaurosisMutationMuscular Dystrophy, DuchenneRetinitis PigmentosaCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesChromosome MappingMuscular Dystrophy, AnimalGenetic LinkageEye ProteinsFundus OculiMolecular Sequence DataHomozygoteFuchs' Endothelial DystrophyPhenotypeConsanguinityRetinal DiseasesLaurence-Moon SyndromeGenes, RecessiveBase SequenceEye Diseases, HereditaryPhotoreceptor Cells, VertebrateRetinaAmino Acid SequencePeripherinsHaplotypesBlindnessMuscular Dystrophy, FacioscapulohumeralDystrophinGenotypeGenetic MarkersDNA Mutational AnalysisPigment Epithelium of EyeBardet-Biedl SyndromeMicrophthalmosPhotoreceptor CellsNight BlindnessGenesAllelesAlstrom SyndromeDark AdaptationVisual AcuityRetinal Pigment EpitheliumMuscular Dystrophy, Emery-DreifussGenes, DominantFluorescein AngiographyMice, Inbred mdxRetinal Rod Photoreceptor CellsDNAUsher SyndromesSyndromeOptic Atrophy, Hereditary, LeberMacular DegenerationMutation, MissenseRetinal Cone Photoreceptor CellsChoroid DiseasesNeuroaxonal DystrophiesOptic Atrophies, HereditaryCodon, NonsenseExonsOptic Disk DrusenSarcoglycansKidney Diseases, CysticLipofuscinRats, Mutant StrainsVisual FieldsHeteroduplex AnalysisTomography, Optical CoherenceRhodopsinExomeMuscular Dystrophy, OculopharyngealDystroglycansVisual Field TestsAge of OnsetReflex Sympathetic DystrophyHeterozygoteVision DisordersPolymorphism, Single-Stranded ConformationalAbnormalities, MultipleUtrophinOphthalmoscopyVitelliform Macular DystrophyLod ScoreFrameshift MutationNerve Tissue ProteinsMuscle, SkeletalIntermediate Filament ProteinsIntellectual DisabilityGenetic TestingRod OpsinsCarrier ProteinsMembrane ProteinsRod Cell Outer SegmentATP-Binding Cassette Transporters