Muscular Dystrophy, Emery-DreifussMuscular Dystrophy, DuchenneMuscular DystrophiesThymopoietinsMuscular Dystrophy, AnimalDystrophinNeurologyMice, Inbred mdxUtrophinMuscular Dystrophies, Limb-GirdleMyotonic DystrophyMuscular Dystrophy, FacioscapulohumeralSarcoglycansMuscle, SkeletalDystroglycansCorneal Dystrophies, HereditaryHeterozygote DetectionMuscular Dystrophy, OculopharyngealDystrophin-Associated ProteinsSarcolemmaCreatine KinaseMuscle Fibers, SkeletalX ChromosomeMusclesExonsPedigreeFuchs' Endothelial DystrophyMyoblastsDystrophin-Associated Protein ComplexMuscle ProteinsNeuromuscular DiseasesRetinal DystrophiesCollagen Type VIDiaphragmCaveolin 3Genetic TherapyDisease Models, AnimalCardiomyopathiesMutationCytoskeletal ProteinsMuscular DiseasesMuscle StrengthRegenerationLamininPregnenedionesGenetic LinkagePhenotypeMorpholinosMice, Inbred C57BLChromosomes, Human, Pair 4Lamin Type APoly(A)-Binding Protein IIHeterozygoteMuscle DevelopmentDependovirusSatellite Cells, Skeletal MuscleMuscle WeaknessNervous System DiseasesMyostatinPrenatal DiagnosisGenes, RecessiveMembrane ProteinsMyoblasts, SkeletalMolecular Sequence DataGenetic CounselingNeuroaxonal DystrophiesSyndromeGlycerol KinaseSarcoglycanopathiesImmunohistochemistryWalker-Warburg SyndromeChromosome MappingScoliosisCalpainChromosome DeletionMuscle CellsDNA Mutational AnalysisMuscle ContractionBase SequenceIntegrin alpha ChainsPolymerase Chain ReactionBiopsyPlectinEvans BlueMice, TransgenicOligonucleotides, AntisenseNitric Oxide Synthase Type IFibrosisCardiomyopathy, DilatedOligoribonucleotides, AntisenseGenetic TestingConsanguinityConnectin