Muscular DystrophiesMuscular Dystrophy, DuchenneMuscular Dystrophy, AnimalDystrophinMyotonic DystrophyMuscular Dystrophies, Limb-GirdleMuscular Dystrophy, FacioscapulohumeralMice, Inbred mdxMuscular Dystrophy, Emery-DreifussSarcoglycansCorneal Dystrophies, HereditaryDystroglycansMuscular Dystrophy, OculopharyngealUtrophinMuscle, SkeletalFuchs' Endothelial DystrophyThymopoietinsRetinal DystrophiesCollagen Type VIPedigreeDystrophin-Associated ProteinsSarcolemmaHeterozygote DetectionCreatine KinaseMuscle ProteinsMyoblastsMuscle Fibers, SkeletalMusclesChromosomes, Human, Pair 4Lamin Type ADystrophin-Associated Protein ComplexLamininExonsCaveolin 3Poly(A)-Binding Protein IIMutationMuscular DiseasesX ChromosomeNeuromuscular DiseasesPhenotypeCytoskeletal ProteinsNeuroaxonal DystrophiesDisease Models, AnimalSarcoglycanopathiesWalker-Warburg SyndromeGenetic LinkageCalpainCardiomyopathiesGenes, RecessivePlectinGenetic TherapyConsanguinityConnectinMuscle DevelopmentRegenerationReflex Sympathetic DystrophyMembrane ProteinsMuscle WeaknessDiaphragmDNA Mutational AnalysisMuscle StrengthVitelliform Macular DystrophyMolecular Sequence DataHeterozygoteChromosome MappingMyositisMyostatinMice, Inbred C57BLGenes, DominantLaminsSatellite Cells, Skeletal MuscleDependovirusBase SequenceMutation, MissenseImmunohistochemistryCardiomyopathy, DilatedElectroretinographyMice, TransgenicMuscular AtrophyTrinucleotide Repeat ExpansionMuscle CellsMyotonic DisordersHomozygoteGlycosylationMyoblasts, SkeletalCreatine Kinase, MM FormMannosyltransferasesBiopsyN-AcetylglucosaminyltransferasesPrenatal DiagnosisMice, KnockoutSyndromeRetinal DegenerationPoly(A)-Binding Protein IMembrane GlycoproteinsMorpholinosGenetic CounselingPolymerase Chain ReactionOxepinsFrameshift Mutation