Myotonic DystrophyMuscular DystrophiesGenes, DominantMyotonic DisordersTrinucleotide Repeat ExpansionPedigreeMuscular Dystrophy, DuchennePolycystic Kidney, Autosomal DominantTrinucleotide RepeatsCorneal Dystrophies, HereditaryMuscular Dystrophy, AnimalMyotoniaMuscular Dystrophy, FacioscapulohumeralMutationGenetic LinkageChromosomes, Human, Pair 19Fuchs' Endothelial DystrophyRNA-Binding ProteinsProtein-Serine-Threonine KinasesDNA Repeat ExpansionRetinal DystrophiesMuscle, SkeletalRetinitis PigmentosaDNA Mutational AnalysisPhenotypeDystrophinLod ScoreBase SequenceMolecular Sequence DataExonsTRPP Cation ChannelsChromosome MappingRepetitive Sequences, Nucleic AcidMyotonia CongenitaAlternative SplicingMuscular Dystrophy, Emery-DreifussMutation, MissenseAge of OnsetMyoblastsCataractAllelesGenetic MarkersHeterozygoteOptic Atrophy, Autosomal DominantLens DiseasesMice, Inbred mdxAnticipation, GeneticHaplotypesPolymerase Chain ReactionRNAChromosomes, Human, 19-20SarcoglycansGenes, RecessiveNeuroaxonal DystrophiesMusclesGenetic TestingRNA SplicingNeuromuscular DiseasesSyndromeMuscle WeaknessDNAFounder EffectMuscular DiseasesDisease Models, AnimalElectroretinography3' Untranslated RegionsMuscular Dystrophy, OculopharyngealEye ProteinsHeterozygote DetectionRNA, MessengerMice, Transgenic