Retinal DystrophiesMuscular DystrophiesRetinal DegenerationMyotonic DystrophyLeber Congenital AmaurosisMuscular Dystrophy, DuchennePedigreeRetinitis PigmentosaCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesMutationGenes, RecessiveMuscular Dystrophy, AnimalEye ProteinsFundus OculiDNA Mutational AnalysisSyndromeGenetic Diseases, InbornConsanguinityFuchs' Endothelial DystrophyRetinal DiseasesProtoporphyria, ErythropoieticLaurence-Moon SyndromePhenotypeGenes, DominantMetabolism, Inborn ErrorsEye Diseases, HereditaryPhotoreceptor Cells, VertebrateRetinaPeripherinsBlindnessMutation, MissenseMuscular Dystrophy, FacioscapulohumeralDystrophinCodon, NonsenseHeterozygoteGenetic LinkageExonsBipolar DisorderGranulomatous Disease, ChronicMolecular Sequence DataBardet-Biedl SyndromePigment Epithelium of EyeHomozygoteMicrophthalmosPhotoreceptor CellsNight BlindnessChromosome MappingFrameshift MutationFerrochelataseGenetic TestingAlstrom SyndromeBase SequenceVisual AcuityDark AdaptationRetinal Pigment EpitheliumMental DisordersAge of OnsetAbnormalities, MultiplePorphyria, HepatoerythropoieticMuscular Dystrophy, Emery-DreifussGenotypeAnxiety DisordersMood DisordersFluorescein AngiographyMice, Inbred mdxDisease Models, AnimalJaundice, Chronic IdiopathicRetinal Rod Photoreceptor CellsIntellectual DisabilityLod ScoreAmino Acid Metabolism, Inborn ErrorsUsher SyndromesOptic Atrophy, Hereditary, LeberLipid Metabolism, Inborn ErrorsHepatolenticular DegenerationPolymorphism, Single-Stranded ConformationalMacular DegenerationRetinal Cone Photoreceptor CellsHemochromatosisNeuroaxonal DystrophiesChoroid DiseasesOptic Atrophies, HereditaryIchthyosisPoint MutationHaplotypesMembrane ProteinsPolymerase Chain ReactionAmino Acid SequenceSarcoglycansOptic Disk DrusenHypophosphatasiaKidney Diseases, CysticRats, Mutant StrainsLipofuscinHeterozygote DetectionHemoglobinopathiesCarrier ProteinsDiagnostic and Statistical Manual of Mental Disorders