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 ChromosomeExonsMusclesPedigreeFuchs' Endothelial DystrophyMyoblastsDystrophin-Associated Protein ComplexMuscle ProteinsNeuromuscular DiseasesRetinal DystrophiesCollagen Type VIDiaphragmCaveolin 3Genetic TherapyDisease Models, AnimalMutationCardiomyopathiesCytoskeletal ProteinsMuscular DiseasesMuscle StrengthRegenerationLamininPregnenedionesGenetic LinkagePhenotypePrenatal DiagnosisMorpholinosMice, Inbred C57BLChromosomes, Human, Pair 4Lamin Type APoly(A)-Binding Protein IIHeterozygoteMuscle DevelopmentDependovirusSatellite Cells, Skeletal MuscleMuscle WeaknessGenes, RecessiveGenetic CounselingMembrane ProteinsMyostatinMolecular Sequence DataBiopsyMyoblasts, SkeletalImmunohistochemistryNeuroaxonal DystrophiesSyndromePolymerase Chain ReactionGlycerol KinaseChromosome MappingSarcoglycanopathiesScoliosisWalker-Warburg SyndromeChromosome DeletionCalpainDNA Mutational AnalysisMuscle CellsBase SequenceMuscle ContractionIntegrin alpha ChainsGenetic TestingPlectinMice, TransgenicEvans BlueOligonucleotides, AntisenseCardiomyopathy, DilatedFibrosisNitric Oxide Synthase Type IOligoribonucleotides, AntisenseConsanguinityElectroretinographyConnectin