Genes, DominantPeriaqueductal GrayPedigreeMutationMolecular Sequence DataMagnetic Resonance ImagingPhenotypeBrainGenetic LinkageBase SequenceAllelesChromosome MappingImage Processing, Computer-AssistedMutation, MissenseLod ScoreDNA Mutational AnalysisGenes, RecessiveOptic Atrophy, Autosomal DominantRetinitis PigmentosaAtrophySocial DominanceSignal TransductionHeterozygoteCell LineGenotypeTransfectionSequence Analysis, DNANerve Fibers, UnmyelinatedCerebral CortexTime FactorsBrain MappingDominance-SubordinationGray Platelet SyndromeHaplotypesPolymerase Chain ReactionFunctional LateralityPoint MutationNerve Fibers, MyelinatedDNA-Binding ProteinsCells, CulturedCrosses, GeneticGenetic MarkersTranscription FactorsSyndromePhylogenyRNA, MessengerSeals, EarlessDNA PrimersGene Expression RegulationModels, BiologicalProtein BindingAmino Acid SubstitutionExonsOvarian FollicleCataractAge of OnsetWolvesImmunodominant EpitopesMice, TransgenicGenetic Predisposition to DiseaseMice, Inbred C57BLNeuronsGenetic HeterogeneityDominance, CerebralPenetranceGenes, LethalGenetic VariationGene ExpressionSpecies SpecificityProtein-Serine-Threonine KinasesEcosystemHomozygoteModels, GeneticTranscription, GeneticProtein Structure, TertiaryPhosphorylationPromoter Regions, GeneticDisease Models, AnimalPolycystic Kidney DiseasesSequence DeletionFrontal LobeEye ProteinsCheirogaleidaeMembrane ProteinsProteinsMicrosatellite RepeatsRecombinant Fusion ProteinsBlotting, WesternTemporal LobeRNA, Ribosomal, 16SFamily HealthOrgan SizePolymorphism, GeneticFrameshift MutationSequence Homology, Amino AcidCase-Control StudiesNeuropsychological TestsDNACADASILNeuroimaging