Huntington DiseaseGenes, DominantPedigreeSerotonin Plasma Membrane Transport ProteinsMutationTelangiectasia, Hereditary HemorrhagicNerve Tissue ProteinsTrinucleotide Repeat ExpansionGenetic LinkagePhenotypeNuclear ProteinsMutation, MissenseDNA Mutational AnalysisTrinucleotide RepeatsMolecular Sequence DataBase SequenceChromosomes, Human, Pair 4Mutant ProteinsDisease Models, AnimalRotarod Performance TestPolycystic Kidney, Autosomal DominantPolymerase Chain ReactionCorpus StriatumMice, TransgenicGenetic Diseases, InbornGenotypeInclusion BodiesGenetic TestingPeptidesBrainAllelesAge of OnsetProtoporphyria, ErythropoieticQuinolinic AcidHeterozygoteGenetic MarkersNeuronsMuscular Dystrophy, FacioscapulohumeralMembrane Transport ProteinsGenes, RecessivePolymorphism, GeneticChorea3-Hydroxyanthranilate 3,4-DioxygenaseRats, TransgenicExonsProdromal SymptomsSerotoninChromosome MappingNeurodegenerative DiseasesWitchcraftCell LineNerve DegenerationPoint MutationAtrophyHaplotypesHomozygoteCaudate NucleusNeostriatumTetrabenazineMythologyTRPP Cation ChannelsQuinolinic AcidsLod ScoreCells, CulturedGene Knock-In TechniquesRetinitis PigmentosaProtein BindingNerve Fibers, UnmyelinatedDopamine and cAMP-Regulated Phosphoprotein 32MitochondriaPutamenGenetic CounselingDisease ProgressionChromosome BandingLipoylationBlotting, WesternOptic Atrophy, Autosomal DominantAmino Acid SequencePC12 CellsGene Expression RegulationHeterozygote DetectionFamilyMagnetic Resonance ImagingDNAPolymorphism, Restriction Fragment LengthNitro CompoundsEarly DiagnosisProtein Structure, TertiaryGenetic Predisposition to DiseaseUbiquitinCataractPolycystic Kidney Diseases