Muscular DystrophiesMuscular Dystrophy, DuchenneMuscular Dystrophy, AnimalDystrophinMyotonic DystrophyMuscular Dystrophies, Limb-GirdleMuscular Dystrophy, FacioscapulohumeralMice, Inbred mdxMuscular Dystrophy, Emery-DreifussSarcoglycansCorneal Dystrophies, HereditaryDystroglycansMuscular Dystrophy, OculopharyngealUtrophinMuscle, SkeletalResearchFuchs' Endothelial DystrophyThymopoietinsRetinal DystrophiesCollagen Type VIPedigreeDystrophin-Associated ProteinsSarcolemmaHeterozygote DetectionCreatine KinaseMuscle ProteinsMyoblastsMuscle Fibers, SkeletalMusclesChromosomes, Human, Pair 4Lamin Type AExonsDystrophin-Associated Protein ComplexLamininCaveolin 3MutationPoly(A)-Binding Protein IIMuscular DiseasesX ChromosomePhenotypeResearch Support as TopicNeuromuscular DiseasesDisease Models, AnimalCytoskeletal ProteinsNeuroaxonal DystrophiesResearch DesignGenetic LinkageSarcoglycanopathiesWalker-Warburg SyndromeEthics, ResearchCalpainCardiomyopathiesResearch PersonnelGenes, RecessivePlectinGenetic TherapyRegenerationConsanguinityConnectinMuscle DevelopmentNursing ResearchMembrane ProteinsMuscle WeaknessReflex Sympathetic DystrophyDNA Mutational AnalysisDiaphragmMuscle StrengthMolecular Sequence DataChromosome MappingHeterozygoteVitelliform Macular DystrophyMice, Inbred C57BLMyostatinMyositisHealth Services ResearchGenes, DominantTranslational Medical ResearchLaminsSatellite Cells, Skeletal MuscleDependovirusBase SequenceImmunohistochemistryMice, TransgenicMutation, MissenseGenetic ResearchCardiomyopathy, DilatedElectroretinographyMuscular AtrophyTrinucleotide Repeat ExpansionMuscle CellsHomozygoteBiopsyGlycosylationPolymerase Chain ReactionMyotonic DisordersSyndromeMyoblasts, SkeletalMice, KnockoutCreatine Kinase, MM FormGenetic Counseling