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  • Molecular assay reagents intended to identify genetic variants associated with primary coenzyme Q10 deficiencies, a collection of genetic diseases caused by loss of function of genes encoding proteins responsible for the synthesis of coenzyme Q10 (ubiquinone). Genetic variants at multiple loci have been associated with primary coenzyme Q10 deficiencies. These reagents are intended to detect various types of genetics changes (e.g. deletions, duplications, insertions, single nucleotide polymorphisms) in multiple primary coenzyme Q10 deficiency-associated loci simultaneously.
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