Trinucleotide Repeat ExpansionTrinucleotide RepeatsFriedreich AtaxiaDNA Repeat ExpansionSpinocerebellar DegenerationsMyotonic DystrophyFragile X SyndromeHuntington DiseaseFragile X Mental Retardation ProteinBase SequenceMolecular Sequence DataMicrosatellite RepeatsIron-Binding ProteinsAllelesNucleotide MotifsMutationRepetitive Sequences, Nucleic AcidTandem Repeat SequencesSpinocerebellar AtaxiasMachado-Joseph DiseaseDNANucleotidesHeredodegenerative Disorders, Nervous SystemAmino Acid MotifsPolymorphism, GeneticMinisatellite RepeatsNucleic Acid ConformationNerve Tissue ProteinsGenomic InstabilityPolymerase Chain ReactionDinucleotide RepeatsGenetic MarkersGenetic VariationSequence Analysis, DNAPedigreeFlap EndonucleasesFrontotemporal DementiaAmino Acid SequenceAnticipation, GeneticInverted Repeat SequencesDNA, SatelliteGenotypeCerebellar AtaxiaAge of OnsetModels, GeneticDNA PrimersRNA-Binding ProteinsIntranuclear Inclusion BodiesGenetic Diseases, InbornChromosome FragilityMuscular Dystrophy, OculopharyngealChromosome MappingPhenotypeHaplotypesGene FrequencyNuclear ProteinsDNA RepairProteinsPeptidesAmyotrophic Lateral SclerosisGenetics, PopulationTranscription, GeneticHeterozygoteGenome, HumanPolymorphism, Single NucleotideNeurodegenerative DiseasesEvolution, MolecularGenetic LinkagePhylogenyDNA-Binding ProteinsExonsRNA, MessengerSaccharomyces cerevisiaeDNA ReplicationCloning, MolecularDNA, PlantReceptors, AndrogenMice, TransgenicRecombination, GeneticCell LineGenes, DominantRepetitive Sequences, Amino AcidDNA Mutational AnalysisMutS Homolog 2 ProteinExpressed Sequence TagsSpecies SpecificityPromoter Regions, GeneticRNASequence DeletionBinding SitesTandem Mass SpectrometrySaccharomyces cerevisiae ProteinsSequence AlignmentNucleic Acid HeteroduplexesMyoclonic Epilepsies, ProgressiveGenetic LociChromosomes, Human, XOligodeoxyribonucleotidesSequence Homology, Nucleic AcidTranscription Factors