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  • Molecular assay reagents intended to identify genetic variants associated with Leigh syndrome, a form of mitochondrial encephalopathy characterized by psychomotor regression early in life. Genetic variants at multiple loci have been associated with Leigh syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Leigh syndrome-associated loci simultaneously.
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