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  • Molecular assay reagents intended to identify genetic variants associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), a mitochondrial disorder associated with defects in the nervous system and the musculature. Genetic variants at multiple loci have been associated with MELAS. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple MELAS-associated loci simultaneously.
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