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  • Molecular assay reagents intended to identify variants 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 various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in the majority of mitochondrial disorder-associated loci simultaneously.
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