Retinitis PigmentosaGenetic Diseases, X-LinkedEye ProteinsPhotoreceptor Cells, VertebrateEye Diseases, HereditaryPhotoreceptor Connecting CiliumElectroretinographyGenes, ModifierX ChromosomeCarrier ProteinsExonsGenes, X-LinkedCiliaChromosomes, Human, XPedigreeOpen Reading FramesGenetic LinkageRetinaMutationGuanine Nucleotide Exchange FactorsCyclic Nucleotide Phosphodiesterases, Type 6DNA Mutational AnalysisRetinal DegenerationProtein IsoformsRetinal Rod Photoreceptor CellsFluorescent Antibody Technique, IndirectOpsinsProteinsRetinal DiseasesRNA Splice SitesVisual FieldsPhenotypeIntracellular Signaling Peptides and ProteinsAlternative SplicingPolymorphism, Single-Stranded ConformationalDark AdaptationMolecular Sequence DataFundus OculiReverse Transcriptase Polymerase Chain ReactionRNA SplicingRhodopsinHeterozygoteCentriolesCOS CellsSequence Analysis, DNAFrameshift MutationMembrane ProteinsRetinal Cone Photoreceptor CellsImmunoblottingDog DiseasesAmino Acid SequenceTwo-Hybrid System TechniquesMice, Inbred C57BLPolymerase Chain ReactionGenetic HeterogeneityCentrosomeChromosomes, Human, Pair 14Genetic TestingSequence DeletionMice, TransgenicVisual AcuityGenes, DominantMutation, MissenseCattleTissue DistributionGenetic VariationSubcellular FractionsDogsHaplotypesGene Knockdown TechniquesPolymorphism, GeneticGenotypePrecipitin TestsConserved SequenceTransgenesGene DeletionGlutathione TransferaseDisease Models, AnimalCell NucleolusImmunohistochemistryMicroscopy, ElectronTransfectionProtein TransportBase SequenceSequence Homology, Amino AcidElectrophoretic Mobility Shift AssayIntronsPoint MutationCercopithecus aethiopsProtein BindingChromosome MappingSeverity of Illness IndexMicroscopy, FluorescenceDNA, ComplementaryCell LineCloning, MolecularDNA PrimersAnimals, NewbornGene Expression RegulationGene Expression