Retinal DystrophiesMuscular DystrophiesDystrophinMyotonic DystrophyMuscular Dystrophy, DuchenneGenes, DominantCorneal Dystrophies, HereditaryRetinal DegenerationPedigreeMuscular Dystrophy, AnimalRetinitis PigmentosaLeber Congenital AmaurosisX ChromosomeElectroretinographyFuchs' Endothelial DystrophyPolycystic Kidney, Autosomal DominantEye ProteinsMusclesMuscular Dystrophy, Facioscapulohumeralcis-trans-IsomerasesMutationFundus OculiGenes, RecessiveDNA Mutational AnalysisGenetic LinkageConsanguinityMuscular Dystrophy, Emery-DreifussRetinal DiseasesEye Diseases, HereditaryPhenotypePeripherinsMutation, MissensePhotoreceptor Cells, VertebrateLod ScoreMice, Inbred mdxLaurence-Moon SyndromeRetinaSyndromeNeuroaxonal DystrophiesBlindnessSarcoglycansChromosome MappingExonsNight BlindnessMolecular Sequence DataMicrophthalmosHeterozygotePigment Epithelium of EyeMuscular Dystrophy, OculopharyngealVisual AcuityDark AdaptationPhotoreceptor CellsCodon, NonsenseMacular DegenerationAge of OnsetFluorescein AngiographyHaplotypesBardet-Biedl SyndromeDystroglycansVitelliform Macular DystrophyReflex Sympathetic DystrophyTRPP Cation ChannelsBase SequenceMuscle, SkeletalFrameshift MutationUtrophinRetinal Rod Photoreceptor CellsAlstrom SyndromeRetinal Pigment EpitheliumRetinal Cone Photoreceptor CellsChoroid DiseasesAbnormalities, MultipleRhodopsinPolymorphism, Single-Stranded ConformationalHomozygoteGenetic TestingKidney Diseases, CysticGenotypeOptic Atrophies, HereditaryOptic Atrophy, Autosomal DominantOptic Atrophy, Hereditary, LeberExomePolymerase Chain ReactionUsher SyndromesMembrane ProteinsVisual FieldsPoint MutationDisease Models, AnimalHeteroduplex AnalysisChromosomes, Human, Pair 4Rats, Mutant StrainsNerve Tissue ProteinsAmino Acid SequenceIntermediate Filament ProteinsLipofuscinTomography, Optical CoherenceGenetic MarkersOptic Disk DrusenNails, MalformedTrinucleotide Repeat Expansion