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