Muscular DystrophiesMuscular Dystrophy, DuchenneMuscular Dystrophy, AnimalDystrophinMice, Inbred mdxBiopsyMuscular Dystrophies, Limb-GirdleMyotonic DystrophyMuscular Dystrophy, FacioscapulohumeralMuscular Dystrophy, Emery-DreifussUtrophinSarcoglycansDystroglycansCorneal Dystrophies, HereditaryMuscle, SkeletalMuscular Dystrophy, OculopharyngealHeterozygote DetectionBiopsy, NeedleFuchs' Endothelial DystrophyDystrophin-Associated ProteinsSarcolemmaPedigreeThymopoietinsCreatine KinaseMuscle Fibers, SkeletalMusclesRetinal DystrophiesCollagen Type VIExonsMyoblastsMuscle ProteinsX ChromosomeDystrophin-Associated Protein ComplexNeuromuscular DiseasesCaveolin 3MutationLamininMuscular DiseasesDisease Models, AnimalCardiomyopathiesChromosomes, Human, Pair 4Lamin Type ACytoskeletal ProteinsPhenotypeGenetic LinkagePoly(A)-Binding Protein IIGenetic TherapyDiaphragmRegenerationMuscle StrengthNeuroaxonal DystrophiesSarcoglycanopathiesGenes, RecessiveWalker-Warburg SyndromeHeterozygoteMuscle DevelopmentCalpainPregnenedionesMuscle WeaknessMice, Inbred C57BLImmunohistochemistryMembrane ProteinsMolecular Sequence DataMyositisSatellite Cells, Skeletal MuscleDNA Mutational AnalysisPlectinMyostatinDependovirusMorpholinosPrenatal DiagnosisChromosome MappingPolymerase Chain ReactionGenetic CounselingConsanguinityConnectinBase SequenceReflex Sympathetic DystrophyMyoblasts, SkeletalCardiomyopathy, DilatedSyndromeMuscle CellsVitelliform Macular DystrophyChromosome DeletionMice, TransgenicGenetic TestingElectroretinographyIntegrin alpha ChainsGenes, DominantGene DeletionMuscle ContractionFibrosisEvans BlueGlycerol KinaseLaminsFrameshift MutationBlotting, WesternCodon, NonsenseMice, KnockoutScoliosis