Muscular DystrophiesMuscular Dystrophy, DuchenneMuscular Dystrophy, AnimalDystrophinMyotonic DystrophyMuscular Dystrophies, Limb-GirdleMice, Inbred mdxMuscular Dystrophy, FacioscapulohumeralMuscular Dystrophy, Emery-DreifussSarcoglycansUtrophinDystroglycansCorneal Dystrophies, HereditaryMuscular Dystrophy, OculopharyngealMuscle, SkeletalFuchs' Endothelial DystrophyHeterozygote DetectionThymopoietinsRetinal DystrophiesCollagen Type VIPedigreeDystrophin-Associated ProteinsSarcolemmaCreatine KinaseMuscle Fibers, SkeletalMusclesMuscle ProteinsMyoblastsExonsX ChromosomeDystrophin-Associated Protein ComplexMutationCaveolin 3LamininNeuromuscular DiseasesChromosomes, Human, Pair 4Lamin Type AMuscular DiseasesPoly(A)-Binding Protein IIPhenotypeCytoskeletal ProteinsDisease Models, AnimalGenetic LinkageCardiomyopathiesNeuroaxonal DystrophiesGenetic TherapySarcoglycanopathiesWalker-Warburg SyndromeCalpainDiaphragmRegenerationGenes, RecessiveMolecular Sequence DataMuscle StrengthMuscle DevelopmentPlectinMembrane ProteinsMuscle WeaknessHeterozygoteMice, Inbred C57BLDNA Mutational AnalysisConsanguinityConnectinBase SequenceMyostatinReflex Sympathetic DystrophyMyositisChromosome MappingSatellite Cells, Skeletal MuscleDependovirusPregnenedionesVitelliform Macular DystrophyMorpholinosPrenatal DiagnosisImmunohistochemistryGenetic CounselingGenes, DominantCardiomyopathy, DilatedMyoblasts, SkeletalLaminsMice, TransgenicMuscle CellsSyndromePolymerase Chain ReactionElectroretinographyBiopsyMice, KnockoutMutation, MissenseDNAMembrane GlycoproteinsIntegrin alpha ChainsGenetic TestingEvans BlueGene DeletionFrameshift MutationAmino Acid SequenceMuscular AtrophyCodon, NonsenseTrinucleotide Repeat ExpansionMuscle Contraction