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  • Molecular assay reagents intended to identify gene variants associated with nemaline myopathy, a form of muscular dystrophy mainly affecting the muscles of the face, neck, and limbs. Genetic variants at multiple loci have been associated with nemaline myopathy. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple nemaline myopathy-associated loci simultaneously.
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