Muscular DystrophiesMuscular Dystrophy, DuchenneMuscular Dystrophy, AnimalDystrophinMice, Inbred mdxMuscular Dystrophies, Limb-GirdleMyotonic DystrophyMuscular Dystrophy, FacioscapulohumeralMuscular Dystrophy, Emery-DreifussUtrophinSarcoglycansDystroglycansCorneal Dystrophies, HereditaryMuscle, SkeletalMuscular Dystrophy, OculopharyngealHeterozygote DetectionFuchs' Endothelial DystrophyDystrophin-Associated ProteinsSarcolemmaThymopoietinsPedigreeCreatine KinaseMuscle Fibers, SkeletalRetinal DystrophiesCollagen Type VIMusclesExonsMyoblastsX ChromosomeMuscle ProteinsDystrophin-Associated Protein ComplexNeuromuscular DiseasesCaveolin 3MutationLamininMuscular DiseasesDisease Models, AnimalChromosomes, Human, Pair 4Lamin Type ACytoskeletal ProteinsCardiomyopathiesPhenotypeGenetic LinkagePoly(A)-Binding Protein IIGenetic TherapyDiaphragmRegenerationMuscle StrengthNeuroaxonal DystrophiesSarcoglycanopathiesWalker-Warburg SyndromeGenes, RecessiveMuscle DevelopmentCalpainHeterozygotePregnenedionesMice, Inbred C57BLMuscle WeaknessMembrane ProteinsPlectinMolecular Sequence DataSatellite Cells, Skeletal MuscleMyostatinDependovirusMorpholinosMyositisDNA Mutational AnalysisPrenatal DiagnosisChromosome MappingGenetic CounselingConsanguinityConnectinReflex Sympathetic DystrophyImmunohistochemistryMyoblasts, SkeletalCardiomyopathy, DilatedBase SequenceSyndromeMuscle CellsPolymerase Chain ReactionVitelliform Macular DystrophyBiopsyChromosome DeletionMice, TransgenicElectroretinographyGenetic TestingIntegrin alpha ChainsEvans BlueGlycerol KinaseGenes, DominantGene DeletionLaminsMuscle ContractionFrameshift MutationCodon, NonsenseMice, KnockoutScoliosisMembrane GlycoproteinsBlotting, WesternIntellectual Disability