Retinitis PigmentosaCytomegalovirus RetinitisElectroretinographyEye ProteinsRhodopsinRetinitisRetinal DegenerationGenes, DominantPhotoreceptor Cells, VertebratePedigreeGenes, RecessiveRetinaPeripherinsGenetic Diseases, X-LinkedDark AdaptationFundus OculiVisual AcuityPhotoreceptor CellsCyclic Nucleotide Phosphodiesterases, Type 6Retinal Rod Photoreceptor CellsVisual FieldsUsher SyndromesRetinal Cone Photoreceptor CellsMutationNight BlindnessGenetic LinkageDNA Mutational AnalysisRod OpsinsBlindnessConsanguinityVisual Field TestsX ChromosomeExonsMutation, MissenseEye Diseases, HereditaryFluorescein AngiographyTomography, Optical CoherenceIMP DehydrogenaseHomozygoteMolecular Sequence DataLaurence-Moon SyndromeRetinal DiseasesCarbonic Anhydrase IVLeber Congenital AmaurosisRibonucleoprotein, U4-U6 Small NuclearRetinal Photoreceptor Cell Outer SegmentTetraspaninsVision DisordersFovea CentralisLod ScorePhenotypeIntermediate Filament ProteinsPolymorphism, Single-Stranded ConformationalPhotoreceptor Connecting CiliumChromosome MappingSensory ThresholdsOpsinsFrameshift MutationDisease Models, AnimalGenes, X-Linkedcis-trans-IsomerasesRetinal DysplasiaMacula LuteaAtaxiaOptic Atrophy, Hereditary, LeberHeterozygoteAmino Acid SequenceBase SequencePhosphenesSyndromeEye Infections, ViralCodon, NonsenseVision TestsVision, OcularBardet-Biedl SyndromeRetinal DystrophiesPolymerase Chain ReactionSequence Analysis, DNACiliaOphthalmoscopyVision, LowPoint MutationRats, TransgenicVisual ProsthesisGenotypeLightRod Cell Outer SegmentOphthalmoscopesElectrooculographyOptic Atrophies, HereditaryCarrier ProteinsRNA SplicingFoscarnetRetinal Bipolar CellsRetinal Pigment EpitheliumArrestinGenetic HeterogeneityChromosomes, Human, Pair 19Pigment Epithelium of EyeDependovirus