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  • Molecular assay reagents intended to identify deletions and duplications in the majority of genes known to be associated with mitochondrial disorders, a collection of conditions associated with deficits in the cellular organelle known as the mitochondria. Genetic variants at multiple loci in both the mitochondrial and nuclear genome have been associated with mitochondrial disorders. These reagents are intended to detect deletions and duplications in the majority of mitochondrial disorder-associated loci simultaneously.
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