PhenotypeMutationPedigreeGenotypeProgeriaDiseaseMolecular Sequence DataDisease Models, AnimalGenetic Predisposition to DiseaseDNA Mutational AnalysisGenetic LinkageAllelesBase Sequencebeta-Hexosaminidase beta ChainMice, TransgenicGenes, DominantMutation, MissensePolymorphism, Single NucleotideManebAmino Acid SequenceChromosome MappingLamin Type ANuclear Receptor Subfamily 2, Group C, Member 2Mice, Inbred C57BLPoint MutationHeterozygoteExonsHaplotypesGenes, RecessiveMice, KnockoutPolymerase Chain ReactionMuscular Atrophy, SpinalGenetic VariationGenetic Association StudiesRetinitis PigmentosaEye ProteinsGenetic Diseases, InbornPrenylationConsanguinityMitochondrial DiseasesGene Expression ProfilingHomozygoteCrosses, GeneticLod ScoreGenome-Wide Association StudyModels, GeneticPolymorphism, GeneticEye Diseases, HereditaryCells, CulturedGenome, HumanHuntington DiseaseHyperkeratosis, EpidermolyticGene Expression RegulationGene DeletionAge of OnsetAmino Acid SubstitutionPenetranceSequence Analysis, DNAPrPSc ProteinsCell DifferentiationMice, Mutant StrainsGene ExpressionHeredodegenerative Disorders, Nervous SystemPolymorphism, Single-Stranded ConformationalNuclear ProteinsSignal TransductionGenetic MarkersRNA, MessengerSyndromeCrohn DiseaseDNA PrimersMice, CongenicImmunohistochemistryCell LineRetinal DegenerationInheritance PatternsHirschsprung DiseaseReverse Transcriptase Polymerase Chain ReactionFamily HealthDNA, MitochondrialComputational BiologyTranscription FactorsPrionsPeripherinsMutant ProteinsMembrane ProteinsGene Regulatory NetworksDNA Repeat ExpansionCase-Control StudiesModels, BiologicalFibroblastsGene FrequencyPrion DiseasesOligonucleotide Array Sequence AnalysisDisease ProgressionDatabases, GeneticBlotting, WesternGenetic TestingTransgenesMice, Inbred CFTR