Muscular Dystrophy, DuchenneMuscular DystrophiesDystrophinMuscular Dystrophy, AnimalMice, Inbred mdxUtrophinMuscular Dystrophies, Limb-GirdleMyotonic DystrophyMuscular Dystrophy, FacioscapulohumeralSarcoglycansMuscular Dystrophy, Emery-DreifussMuscle, SkeletalDystroglycansHeterozygote DetectionCorneal Dystrophies, HereditaryMuscular Dystrophy, OculopharyngealDystrophin-Associated ProteinsSarcolemmaCreatine KinaseMuscle Fibers, SkeletalX ChromosomeExonsMusclesPedigreeMyoblastsNeuromuscular DiseasesDystrophin-Associated Protein ComplexFuchs' Endothelial DystrophyMuscle ProteinsThymopoietinsDiaphragmRetinal DystrophiesGenetic TherapyCollagen Type VICaveolin 3Disease Models, AnimalCardiomyopathiesPregnenedionesMuscle StrengthCytoskeletal ProteinsMutationRegenerationMuscular DiseasesGenetic LinkageLamininMorpholinosPhenotypeMice, Inbred C57BLHeterozygoteDependovirusSatellite Cells, Skeletal MuscleChromosomes, Human, Pair 4Lamin Type AMuscle DevelopmentMuscle WeaknessPoly(A)-Binding Protein IIPrenatal DiagnosisGenetic CounselingMyostatinMyoblasts, SkeletalGlycerol KinaseMembrane ProteinsMolecular Sequence DataGenes, RecessiveChromosome DeletionScoliosisImmunohistochemistryChromosome MappingSyndromeNeuroaxonal DystrophiesMuscle CellsMuscle ContractionPolymerase Chain ReactionSarcoglycanopathiesIntegrin alpha ChainsWalker-Warburg SyndromeBase SequenceBiopsyCalpainDNA Mutational AnalysisOligonucleotides, AntisenseNitric Oxide Synthase Type IFibrosisEvans BlueOligoribonucleotides, AntisenseCardiomyopathy, DilatedMice, TransgenicGenetic TestingGene DeletionGenetic VectorsProjective TechniquesPlectinBlotting, WesternElectroretinographyInjections, IntramuscularMyositisDNACodon, NonsenseMazindolIntellectual Disability