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  • Molecular assay reagents intended to identify genetic variants associated with mitochondrial encephalopathy, forms of encephalopathy whose underlying cause is a deficit in mitochondrial function. Genetic variants at multiple loci have been associated with mitochondrial encephalopathy. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple mitochondrial encephalopathy-associated loci simultaneously.
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