Retinal DystrophiesLeber Congenital AmaurosisGenes, RecessiveMuscular DystrophiesRetinal DegenerationAge of OnsetMyotonic DystrophyPedigreeArm BonesRetinitis PigmentosaMuscular Dystrophy, DuchenneConsanguinityCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesDwarfism, PituitaryMutationDNA Mutational AnalysisEye ProteinsDystonic DisordersFundus OculiMuscular Dystrophy, AnimalSleep-Wake Transition DisordersRetinal DiseasesFuchs' Endothelial DystrophyEye Diseases, HereditaryLaurence-Moon SyndromePhotoreceptor Cells, VertebrateRetinaBlindnessSyndromePeripherinsDystrophinMuscular Dystrophy, FacioscapulohumeralPhenotypeHomozygoteBardet-Biedl SyndromeHuman Growth HormoneMutation, MissenseMicrophthalmosGenes, DominantNight BlindnessPigment Epithelium of EyeGenetic LinkagePhotoreceptor CellsCodon, NonsenseAlstrom SyndromeExonsVisual AcuityChromosome MappingDark AdaptationRetinal Pigment EpitheliumLod ScoreAbnormalities, MultipleHeterozygoteUsher SyndromesFluorescein AngiographyMolecular Sequence DataSarcoglycansMuscular Dystrophy, Emery-DreifussRetinal Rod Photoreceptor CellsOptic Atrophy, Hereditary, LeberMice, Inbred mdxKidney Diseases, CysticDiabetes Mellitus, Type 1Neuroaxonal DystrophiesMacular DegenerationFrameshift MutationOptic Atrophies, HereditaryRetinal Cone Photoreceptor CellsExomePolycystic Kidney, Autosomal RecessiveHaplotypesIntellectual DisabilityBase SequenceChoroid DiseasesRats, Mutant StrainsPolymorphism, Single-Stranded ConformationalGenotype