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  • Molecular assay reagents intended to identify gene variants associated with myofibrillar myopathies, a collection of muscular dystrophies mainly affecting skeletal muscles whose signs and symptoms typically arise in mid-adulthood. Genetic variants at multiple loci have been associated with myofibrillar myopathies. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple myofibrillar myopathy-associated loci simultaneously.
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