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  • Molecular assay reagents intended to identify deletions or duplications of genes associated with catecholaminergic polymorphic ventricular tachycardia, a ventricular tachycardia characterized by episodic syncope (i.e., fainting) and the absence of structural heart defects. Genetic variants at multiple loci have been associated with catecholaminergic polymorphic ventricular tachycardia. These reagents are intended to detect deletions and duplications in multiple catecholaminergic polymorphic ventricular tachycardia-associated loci simultaneously.
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