Retinal DystrophiesMuscular DystrophiesDystrophinMyotonic DystrophyMuscular Dystrophy, DuchenneCorneal Dystrophies, HereditaryRetinal DegenerationMuscular Dystrophy, AnimalLeber Congenital AmaurosisX ChromosomeRetinitis PigmentosaMutation, MissenseFuchs' Endothelial DystrophyMutationPoint MutationPedigreeElectroretinographyMusclescis-trans-IsomerasesMuscular Dystrophy, FacioscapulohumeralEye ProteinsFundus OculiGenes, RecessiveConsanguinityDNA Mutational AnalysisFrameshift MutationRetinal DiseasesMuscular Dystrophy, Emery-DreifussMice, Inbred mdxEye Diseases, HereditaryLaurence-Moon SyndromePhotoreceptor Cells, VertebrateExonsPeripherinsRetinaNeuroaxonal DystrophiesGenes, DominantBlindnessSarcoglycansPhenotypeHeterozygoteCodon, NonsenseMolecular Sequence DataNight BlindnessBase SequenceSyndromePigment Epithelium of EyeMicrophthalmosBardet-Biedl SyndromeDystroglycansVisual AcuityHomozygoteMuscular Dystrophy, OculopharyngealPhotoreceptor CellsPolymorphism, Single-Stranded ConformationalReflex Sympathetic DystrophyGenetic LinkageDark AdaptationVitelliform Macular DystrophyChromosome MappingPolymerase Chain ReactionGerm-Line MutationMuscle, SkeletalAlstrom SyndromeMacular DegenerationUtrophinRetinal Pigment EpitheliumFluorescein AngiographyRetinal Cone Photoreceptor CellsGenotypeRetinal Rod Photoreceptor CellsGenetic TestingAmino Acid SequenceOptic Atrophy, Hereditary, LeberAmino Acid SubstitutionUsher SyndromesOptic Atrophies, HereditaryAge of OnsetExomeChoroid DiseasesMembrane ProteinsKidney Diseases, CysticSequence Analysis, DNAAbnormalities, MultipleHeterozygote DetectionHeteroduplex AnalysisRats, Mutant StrainsLipofuscinVisual FieldsOptic Disk DrusenCarrier ProteinsAllelesLod ScoreTomography, Optical CoherenceDisease Models, AnimalMutation RateNerve Tissue ProteinsRhodopsinIntellectual DisabilityProteins