Retinitis PigmentosaRetinal DystrophiesElectroretinographyRetinal DegenerationEye ProteinsCytomegalovirus RetinitisPedigreeMuscular DystrophiesRhodopsinPhotoreceptor Cells, VertebrateGenes, RecessiveMutationGenes, DominantFundus OculiLeber Congenital AmaurosisMyotonic DystrophyRetinaMutation, MissenseRetinitisPeripherinsPoint MutationDark AdaptationPhotoreceptor CellsDNA Mutational AnalysisVisual Acuitycis-trans-IsomerasesConsanguinityMuscular Dystrophy, DuchenneRetinal Rod Photoreceptor CellsUsher SyndromesGenetic Diseases, X-LinkedNight BlindnessBlindnessVisual FieldsRetinal Cone Photoreceptor CellsEye Diseases, HereditaryCorneal Dystrophies, HereditaryGenetic LinkageRetinal DiseasesLaurence-Moon SyndromeExonsFrameshift MutationCyclic Nucleotide Phosphodiesterases, Type 6Rod OpsinsMolecular Sequence DataMuscular Dystrophy, AnimalVisual Field TestsHomozygotePhenotypeFluorescein AngiographyPolymorphism, Single-Stranded ConformationalCodon, NonsenseHeterozygoteBardet-Biedl SyndromeX ChromosomeBase SequenceTomography, Optical CoherenceChromosome MappingSyndromeOptic Atrophy, Hereditary, LeberPigment Epithelium of EyeAmino Acid SequencePolymerase Chain ReactionLod ScoreFuchs' Endothelial DystrophyRetinal Pigment EpitheliumVision DisordersIntermediate Filament ProteinsMicrophthalmosGenotypeOptic Atrophies, HereditarySequence Analysis, DNADisease Models, AnimalMacular DegenerationGenetic TestingCarrier ProteinsOptic Disk DrusenAmino Acid SubstitutionOphthalmoscopyDystrophinMuscular Dystrophy, FacioscapulohumeralIMP DehydrogenaseMembrane ProteinsKidney Diseases, CysticExomeAge of OnsetTetraspaninsNerve Tissue ProteinsCarbonic Anhydrase IVVision, OcularRod Cell Outer SegmentHeteroduplex AnalysisRibonucleoprotein, U4-U6 Small NuclearFovea CentralisRetinal Photoreceptor Cell Outer SegmentPhotoreceptor Connecting CiliumAllelesLightHaplotypesProteins