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  • Molecular assay reagents intended to identify variants in the majority of genes known to be associated with muscular dystrophies, a collection of neuromuscular diseases characterized by progressive weakening and degeneration of skeletal muscles. Genetic variants at multiple loci have been associated with muscular dystrophies. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in the majority of muscular dystrophy-associated loci simultaneously.
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