Retinal DystrophiesMuscular DystrophiesRetinal DegenerationMutationMyotonic DystrophyLeber Congenital AmaurosisMutation, MissensePoint MutationMuscular Dystrophy, DuchenneRetinitis PigmentosaPedigreeCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesEye ProteinsDNA Mutational AnalysisMuscular Dystrophy, AnimalFundus OculiGenes, RecessiveConsanguinityFrameshift MutationPhenotypeFuchs' Endothelial DystrophyRetinal DiseasesExonsLaurence-Moon SyndromeHeterozygoteEye Diseases, HereditaryCodon, NonsensePhotoreceptor Cells, VertebrateRetinaPeripherinsBase SequenceMolecular Sequence DataBlindnessGenetic TestingHomozygoteDystrophinMuscular Dystrophy, FacioscapulohumeralPolymorphism, Single-Stranded ConformationalGenotypeSyndromeGenes, DominantPolymerase Chain ReactionMicrophthalmosBardet-Biedl SyndromePigment Epithelium of EyeNight BlindnessAmino Acid SubstitutionSequence Analysis, DNAPhotoreceptor CellsGerm-Line MutationGenetic LinkageChromosome MappingAlstrom SyndromeAmino Acid SequenceDark AdaptationVisual AcuityRetinal Pigment EpitheliumAge of OnsetAllelesMuscular Dystrophy, Emery-DreifussOptic Atrophy, Hereditary, LeberUsher SyndromesMice, Inbred mdxMembrane ProteinsRetinal Rod Photoreceptor CellsFluorescein AngiographyOptic Atrophies, HereditaryDisease Models, AnimalExomeRetinal Cone Photoreceptor CellsMacular DegenerationCarrier ProteinsGenetic Predisposition to DiseaseNerve Tissue ProteinsNeuroaxonal DystrophiesChoroid DiseasesSarcoglycansKidney Diseases, CysticHeteroduplex AnalysisOptic Disk DrusenRats, Mutant StrainsMutation RateAbnormalities, MultipleLipofuscinVisual FieldsRhodopsinDNA PrimersFamily HealthTomography, Optical CoherenceFructose-1,6-Diphosphatase DeficiencyHaplotypesProteinsLod ScoreDystroglycansPolymorphism, Single NucleotideMice, Inbred C57BLCell LineIntellectual Disability