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Molecular assay reagents intended to identify deletions and duplications in genes associated with mitochondrial cardiomyopathy, forms of hereditary cardiomyopathy whose underlying cause is a deficit in mitochondrial function. Genetic variants at multiple loci have been associated with mitochondrial cardiomyopathy. These reagents are intended to detect deletions and duplications in multiple mitochondrial cardiomyopathy-associated loci simultaneously.
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