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  • Molecular assay reagents intended to identify gene variants associated with nephrotic syndrome, a group of symptoms caused by kidney damage including proteinuria, hypoalbuminemia, and edema. Genetic variants at multiple loci have been associated with nephrotic syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple nephrotic syndrome-associated loci simultaneously.
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