Muscular DystrophiesMuscular Dystrophy, DuchenneMuscular Dystrophy, AnimalDystrophinMice, Inbred mdxMyotonic DystrophyMuscle, SkeletalUtrophinMuscular Dystrophies, Limb-GirdleMuscular Dystrophy, FacioscapulohumeralSarcoglycansMuscular Dystrophy, Emery-DreifussDystroglycansCorneal Dystrophies, HereditaryHeterozygote DetectionMuscular Dystrophy, OculopharyngealDystrophin-Associated ProteinsSarcolemmaCreatine KinaseMuscle Fibers, SkeletalX ChromosomeMusclesExonsMutationPedigreeFuchs' Endothelial DystrophyMyoblastsDystrophin-Associated Protein ComplexMuscle ProteinsNeuromuscular DiseasesThymopoietinsRetinal DystrophiesCollagen Type VIDiaphragmCaveolin 3Genetic TherapyDisease Models, AnimalCardiomyopathiesCytoskeletal ProteinsMuscular DiseasesMuscle StrengthRegenerationLamininPregnenedionesGenetic LinkagePhenotypeMorpholinosMice, Inbred C57BLChromosomes, Human, Pair 4Lamin Type APoly(A)-Binding Protein IIHeterozygoteMuscle DevelopmentDependovirusSatellite Cells, Skeletal MuscleMuscle WeaknessMyostatinPrenatal DiagnosisGenes, RecessiveMembrane ProteinsMyoblasts, SkeletalMolecular Sequence DataGenetic CounselingNeuroaxonal DystrophiesGlycerol KinaseSarcoglycanopathiesImmunohistochemistryWalker-Warburg SyndromeChromosome MappingScoliosisCalpainChromosome DeletionMuscle CellsSyndromeDNA Mutational AnalysisMuscle ContractionBase SequenceIntegrin alpha ChainsPolymerase Chain ReactionBiopsyPlectinEvans BlueMice, TransgenicOligonucleotides, AntisenseNitric Oxide Synthase Type IFibrosisCardiomyopathy, DilatedOligoribonucleotides, AntisenseGenetic TestingConsanguinityConnectinElectroretinographyGenetic VectorsGene DeletionBlotting, WesternCodon, NonsenseReflex Sympathetic DystrophyProjective TechniquesMyositisDNA