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Molecular assay reagents intended to identify gene variants associated with left ventricular noncompaction cardiomyopathy, a form of cardiomyopathy characterized by the failure of the ventricular myocardium (i.e., heart wall muscle) to properly compact, leaving muscular projections (i.e., trabeculations) into the ventricle. Genetic variants at multiple loci have been associated with left ventricular noncompaction cardiomyopathy. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple left ventricular noncompaction cardiomyopathy-associated loci simultaneously.
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