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