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Molecular assay reagents intended to identify gene variants associated with myoclonic epilepsy, a collection of conditions characterized by brief shock-like contractions of muscles or muscle groups. Genetic variants at multiple loci have been associated with myoclonic epilepsy. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple myoclonic epilepsy-associated loci simultaneously.
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