Huntington DiseaseGenes, DominantPedigreeTelangiectasia, Hereditary HemorrhagicMutationNeurodegenerative DiseasesGenetic LinkagePhenotypeMutation, MissenseTrinucleotide Repeat ExpansionDNA Mutational AnalysisTrinucleotide RepeatsNerve Tissue ProteinsChromosomes, Human, Pair 4Base SequenceMolecular Sequence DataPolycystic Kidney, Autosomal DominantPolymerase Chain ReactionGenetic Diseases, InbornDisease Models, AnimalGenetic TestingNuclear ProteinsAge of OnsetQuinolinic AcidProtoporphyria, ErythropoieticHeterozygoteGenetic MarkersAllelesBrainCorpus StriatumMuscular Dystrophy, FacioscapulohumeralGenes, RecessiveChoreaMice, Transgenic3-Hydroxyanthranilate 3,4-DioxygenaseNeuronsRats, TransgenicProdromal SymptomsExonsGenotypeAtrophyNerve DegenerationRotarod Performance TestInclusion BodiesWitchcraftHaplotypesChromosome MappingCaudate NucleusNeostriatumPeptidesHomozygoteTetrabenazineMythologyMutant ProteinsLod ScoreTRPP Cation ChannelsQuinolinic AcidsPoint MutationRetinitis PigmentosaGene Knock-In TechniquesDisease ProgressionNerve Fibers, UnmyelinatedGenetic CounselingPutamenDopamine and cAMP-Regulated Phosphoprotein 32Optic Atrophy, Autosomal DominantChromosome BandingMagnetic Resonance ImagingNitro CompoundsParkinson DiseaseAlzheimer DiseaseLipoylationAutophagyCell DeathFamilyHeterozygote DetectionGenetic Predisposition to DiseaseCerebral CortexEarly DiagnosisCognition DisordersSpinocerebellar Ataxiasalpha-SynucleinCells, CulturedProtein FoldingMitochondriaPolymorphism, Restriction Fragment LengthSpinocerebellar Degenerationstau ProteinsFamily HealthDNACell LineAmyotrophic Lateral SclerosisPolycystic Kidney DiseasesSyndromeMotor ActivityCataractAmino Acid SequenceNeuropsychological TestsAge FactorsCADASIL