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