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Molecular assay reagents intended to identify gene variants 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 multiple neuromuscular disorder-associated loci simultaneously.
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