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Molecular assay reagents intended to identify genetic variants associated with myoclonic epilepsy with ragged-red fibers (MERRF), a mitochondrial disorder associated with defects in the nervous system and the musculature. Genetic variants at multiple loci have been associated with MERRF. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple MERRF-associated loci simultaneously.
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