Retinitis PigmentosaCytomegalovirus RetinitisElectroretinographyEye ProteinsRhodopsinRetinitisRetinal DegenerationPhotoreceptor Cells, VertebrateGenes, DominantPedigreeGenes, 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 NuclearVision DisordersRetinal Photoreceptor Cell Outer SegmentTetraspaninsFovea CentralisLod ScoreIntermediate Filament ProteinsPolymorphism, Single-Stranded ConformationalPhotoreceptor Connecting CiliumPhenotypeChromosome MappingSensory ThresholdsOpsinsFrameshift Mutationcis-trans-IsomerasesGenes, X-LinkedRetinal DysplasiaMacula LuteaDisease Models, AnimalOptic Atrophy, Hereditary, LeberAtaxiaHeterozygoteAmino Acid SequencePhosphenesBase SequenceEye Infections, ViralVision TestsVision, OcularCodon, NonsenseBardet-Biedl SyndromeRetinal DystrophiesSyndromeVision, LowSequence Analysis, DNAPolymerase Chain ReactionOphthalmoscopyCiliaPoint MutationRats, TransgenicVisual ProsthesisLightRod Cell Outer SegmentGenotypeOphthalmoscopesElectrooculographyOptic Atrophies, HereditaryCarrier ProteinsFoscarnetRNA SplicingRetinal Bipolar CellsRetinal Pigment EpitheliumArrestinGenetic HeterogeneityChromosomes, Human, Pair 19Pigment Epithelium of EyeMacular Degeneration