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  • Molecular assay reagents intended to identify genetic variants associated with MERRF/MELAS overlap syndrome, a mitochondrial disorder exhibiting signs and symptoms characteristic of both mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) and myoclonic epilepsy with ragged-red fibers (MERRF). Genetic variants at multiple loci have been associated with MERRF/MELAS overlap syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple MERRF/MELAS overlap syndrome-associated loci simultaneously.
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