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  • Molecular assay reagents intended to identify variants in the majority of genes known to be associated with neuromuscular disorders, a collection of diseases characterized by impairment of skeletal muscle function. Genetic variants at multiple loci have been associated with neuromuscular disorders. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in the majority of neuromuscular disorder-associated loci simultaneously.
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