Muscular Dystrophy, Emery-DreifussMuscular Dystrophy, DuchenneMuscular DystrophiesThymopoietinsMuscular Dystrophy, AnimalDystrophinMice, Inbred mdxUtrophinMuscular Dystrophies, Limb-GirdleMyotonic DystrophyMuscular Dystrophy, FacioscapulohumeralSarcoglycansMuscle, SkeletalDystroglycansCorneal Dystrophies, HereditaryHeterozygote DetectionMuscular Dystrophy, OculopharyngealDystrophin-Associated ProteinsSarcolemmaCreatine KinaseMuscle Fibers, SkeletalX ChromosomePedigreeExonsMusclesFuchs' Endothelial DystrophyMyoblastsNeuromuscular DiseasesDystrophin-Associated Protein ComplexMuscle ProteinsRetinal DystrophiesCollagen Type VIDiaphragmDisease Models, AnimalCaveolin 3Genetic TherapyMutationCardiomyopathiesCytoskeletal ProteinsMuscular DiseasesMuscle StrengthGenetic LinkageRegenerationLamininPhenotypePregnenedionesMorpholinosMice, Inbred C57BLChromosomes, Human, Pair 4Lamin Type AHeterozygotePoly(A)-Binding Protein IIMuscle DevelopmentDependovirusSatellite Cells, Skeletal MuscleMuscle WeaknessGenes, RecessivePrenatal DiagnosisMembrane ProteinsMolecular Sequence DataMyostatinGenetic CounselingMyoblasts, SkeletalNeuroaxonal DystrophiesSyndromeChromosome MappingImmunohistochemistryGlycerol KinaseWalker-Warburg SyndromeSarcoglycanopathiesChromosome DeletionScoliosisCalpainDNA Mutational AnalysisMuscle CellsBase SequencePolymerase Chain ReactionMuscle ContractionBiopsyIntegrin alpha ChainsMice, TransgenicPlectinOligonucleotides, AntisenseEvans BlueGenetic TestingFibrosisNitric Oxide Synthase Type IConsanguinityCardiomyopathy, DilatedOligoribonucleotides, AntisenseGene DeletionGenetic VectorsBlotting, WesternElectroretinographyConnectinIntellectual Disability