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  • Molecular assay reagents intended to identify gene variants associated with paraganglioma-pheochromocytoma syndrome, a syndrome characterized by development of benign tumors that derive from neuroendocrine tissues. Genetic variants at multiple loci have been associated with various forms of paraganglioma-pheochromocytoma syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) multiple paraganglioma-pheochromocytoma syndrome-associated loci simultaneously.
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