Myotonic DystrophyMuscular DystrophiesMuscular Atrophy, SpinalMuscular Dystrophy, DuchenneSpinal Muscular Atrophies of ChildhoodMuscular Dystrophy, AnimalSurvival of Motor Neuron 1 ProteinAtrophySMN Complex ProteinsDystrophinMuscular AtrophyMuscular Dystrophy, FacioscapulohumeralSurvival of Motor Neuron 2 ProteinSpinal CordCorneal Dystrophies, HereditaryMuscular Dystrophies, Limb-GirdleMyotonic DisordersTrinucleotide Repeat ExpansionMice, Inbred mdxMuscular Dystrophy, Emery-DreifussMuscle, SkeletalSarcoglycansRNA-Binding ProteinsFuchs' Endothelial DystrophyTrinucleotide RepeatsDystroglycansMuscular Disorders, AtrophicPedigreeMuscular Dystrophy, OculopharyngealUtrophinBulbo-Spinal Atrophy, X-LinkedRetinal DystrophiesSpinal Cord InjuriesExonsNeuronal Apoptosis-Inhibitory ProteinMyotoniaMotor NeuronsCyclic AMP Response Element-Binding ProteinHeterozygote DetectionMutationDisease Models, AnimalAnterior Horn CellsMusclesMyoblastsNeuromuscular DiseasesPhenotypeMuscle Fibers, SkeletalNerve Tissue ProteinsThymopoietinsMuscle WeaknessDystrophin-Associated ProteinsGenetic LinkageCollagen Type VIMuscular DiseasesChromosomes, Human, Pair 19Alternative SplicingProtein-Serine-Threonine KinasesMice, TransgenicSpinal Cord DiseasesDNA Repeat ExpansionNeuroaxonal DystrophiesBase SequenceMolecular Sequence DataMuscle ProteinsGenes, DominantSarcolemmaElectromyographyGenes, RecessiveCreatine KinaseRNA SplicingOptic AtrophyRepetitive Sequences, Nucleic AcidDNA Mutational AnalysisChromosomes, Human, Pair 5Motor Neuron DiseaseRibonucleoproteins, Small NuclearChromosomes, Human, Pair 4Prenatal DiagnosisX ChromosomePolymerase Chain ReactionChromosome MappingLamin Type AHeterozygoteReflex Sympathetic DystrophyDEAD Box Protein 20Age of OnsetLamininDystrophin-Associated Protein ComplexGenetic TestingCaveolin 3RNA, MessengerAllelesMyotonia CongenitaPoly(A)-Binding Protein IIHomozygoteGenetic CounselingFounder EffectGenetic TherapyVitelliform Macular DystrophySpinal Nerve Roots