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 ComplexMutationNeuromuscular DiseasesDisease Models, AnimalCaveolin 3LamininGenetic TherapyMuscular DiseasesPhenotypeChromosomes, Human, Pair 4Lamin Type ACytoskeletal ProteinsCardiomyopathiesGenetic LinkagePoly(A)-Binding Protein IIDiaphragmRegenerationMuscle StrengthNeuroaxonal DystrophiesMice, Inbred C57BLSarcoglycanopathiesWalker-Warburg SyndromeGenes, RecessiveMuscle DevelopmentCalpainHeterozygotePregnenedionesMuscle WeaknessMultiple MyelomaMolecular Sequence DataMembrane ProteinsTerminally IllPlectinSatellite Cells, Skeletal MuscleImmunohistochemistryMyostatinDependovirusMorpholinosMyositisDNA Mutational AnalysisPrenatal DiagnosisChromosome MappingGenetic CounselingMice, TransgenicConsanguinityConnectinReflex Sympathetic DystrophyMyoblasts, SkeletalCardiomyopathy, DilatedBase SequenceSyndromeMuscle CellsPolymerase Chain ReactionVitelliform Macular DystrophyBiopsyPalliative CareBlotting, WesternDisease ProgressionChromosome DeletionElectroretinographyGenetic VectorsGenetic TestingIntegrin alpha ChainsEvans BlueGlycerol KinaseGenes, DominantGene DeletionLaminsMuscle ContractionFrameshift Mutation