Myopathies, Structural, CongenitalMuscular DystrophiesMuscular Dystrophy, DuchenneDynamin IIMuscular Dystrophy, AnimalDystrophinProtein Tyrosine Phosphatases, Non-ReceptorMuscular DiseasesMice, Inbred mdxNeuromuscular Junction DiseasesNADH Tetrazolium ReductaseMuscle, SkeletalMuscular Dystrophies, Limb-GirdleMyotonic DystrophyMuscular Dystrophy, FacioscapulohumeralMuscular Dystrophy, Emery-DreifussUtrophinSarcoglycansGenes, RecessiveDystroglycansCorneal Dystrophies, HereditaryMutationMuscular Dystrophy, OculopharyngealPhenotypeHeterozygote DetectionFuchs' Endothelial DystrophyDystrophin-Associated ProteinsSarcolemmaThymopoietinsPedigreeCreatine KinaseMuscle Fibers, SkeletalRetinal DystrophiesCollagen Type VIMusclesExonsMyoblastsX ChromosomeMuscle ProteinsDystrophin-Associated Protein ComplexNeuromuscular DiseasesCaveolin 3LamininDisease Models, AnimalChromosomes, Human, Pair 4Lamin Type ACytoskeletal ProteinsCardiomyopathiesGenetic LinkagePoly(A)-Binding Protein IIGenetic TherapyDiaphragmRegenerationMuscle StrengthNeuroaxonal DystrophiesSarcoglycanopathiesWalker-Warburg SyndromeMuscle DevelopmentCalpainHeterozygotePregnenedionesMice, Inbred C57BLMuscle WeaknessMembrane ProteinsPlectinMolecular Sequence DataSatellite Cells, Skeletal MuscleMyostatinDependovirusMorpholinosMyositisDNA Mutational AnalysisPrenatal DiagnosisChromosome MappingGenetic CounselingConsanguinityConnectin