Muscular DystrophiesMuscular Dystrophy, DuchenneMuscular Dystrophy, AnimalMyotonic DystrophyDystrophinMuscular Dystrophy, FacioscapulohumeralCorneal Dystrophies, HereditaryMuscular Dystrophies, Limb-GirdleMice, Inbred mdxMuscular Dystrophy, Emery-DreifussSarcoglycansFuchs' Endothelial DystrophyDystroglycansMuscular Dystrophy, OculopharyngealUtrophinRetinal DystrophiesMuscle, SkeletalThymopoietinsPedigreeCollagen Type VINeuroaxonal DystrophiesDystrophin-Associated ProteinsHeterozygote DetectionSarcolemmaCreatine KinaseMyoblastsMuscle ProteinsMuscle Fibers, SkeletalMusclesMutationExonsChromosomes, Human, Pair 4Lamin Type AReflex Sympathetic DystrophyLamininDystrophin-Associated Protein ComplexCaveolin 3Poly(A)-Binding Protein IIPhenotypeMuscular DiseasesX ChromosomeVitelliform Macular DystrophyNeuromuscular DiseasesGenetic LinkageCytoskeletal ProteinsDisease Models, AnimalGenes, RecessiveSarcoglycanopathiesWalker-Warburg SyndromeCalpainConsanguinityCardiomyopathiesDNA Mutational AnalysisRetinal DegenerationPlectinElectroretinographyGenetic TherapyGenes, DominantMuscle DevelopmentMyotonic DisordersRegenerationRetinitis PigmentosaConnectinTrinucleotide Repeat ExpansionMembrane ProteinsMuscle WeaknessMolecular Sequence DataHeterozygoteChromosome MappingDiaphragmMuscle StrengthMyositisMice, Inbred C57BLMutation, MissenseBase SequenceMyostatinSatellite Cells, Skeletal MuscleLaminsDependovirusHomozygoteFundus OculiCorneal Dystrophy, Juvenile Epithelial of MeesmannMice, TransgenicImmunohistochemistrySyndromeCollagen Type VIIIPolymerase Chain ReactionCardiomyopathy, DilatedMuscular AtrophyKeratoplasty, PenetratingMyoblasts, SkeletalMuscle CellsFrameshift MutationBiopsyMice, KnockoutCorneaCodon, NonsensePrenatal DiagnosisMacular DegenerationGlycosylation