Cardiomyopathy, DilatedCardiomyopathy, HypertrophicPhenotypeCardiomyopathiesPoint MutationMutation, MissenseCardiomyopathy, RestrictiveMutationTakotsubo CardiomyopathyCardiomyopathy, Hypertrophic, FamilialChagas CardiomyopathyPedigreeFrameshift MutationIdiopathic Pulmonary FibrosisMyocardiumCardiomyopathy, AlcoholicGerm-Line MutationEchocardiographyArrhythmogenic Right Ventricular DysplasiaMolecular Sequence DataHeterozygoteBase SequenceGenotypeDNA Mutational AnalysisElectrocardiographyExonsAllelesPolymerase Chain ReactionDiabetic CardiomyopathiesAmino Acid SubstitutionScoliosisAmino Acid SequenceMyocarditisHeart VentriclesVentricular Function, LeftVentricular Dysfunction, LeftHomozygoteArthritis, JuvenileMutation RateHeart FailureHeart SeptumPurpura, Thrombocytopenic, IdiopathicGenetic TestingPolymorphism, Single-Stranded ConformationalMice, TransgenicCodon, NonsenseSequence Analysis, DNASyndromeGenes, DominantHeartMyocytes, CardiacDeath, Sudden, CardiacDisease Models, AnimalMyocardial ContractionGenes, RecessiveGenetic Predisposition to DiseaseCardiac MyosinsChromosome MappingVentricular Outflow ObstructionTachycardia, VentricularMutagenesisGene DeletionStroke VolumeMutagenesis, Site-DirectedSequence DeletionCase-Control StudiesGenetic LinkageTime FactorsMyosin Heavy ChainsTreatment OutcomeDNA PrimersFibrosisCell LineFollow-Up StudiesRNA, MessengerVentricular MyosinsTranscription FactorsPrognosisLamin Type ASignal TransductionCells, CulturedSarcomeresEchocardiography, DopplerMice, Inbred C57BLArrhythmias, CardiacCarrier ProteinsPeripartum PeriodGenetic Complementation TestProtein Structure, TertiaryDNA-Binding ProteinsSuppression, GeneticMice, KnockoutSequence Homology, Amino AcidEndomyocardial FibrosisMembrane ProteinsPulmonary FibrosisEndocardiumRetrospective StudiesBiopsyAge of Onset