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Molecular assay reagents intended to identify gene variants associated with platelet-type bleeding disorders, a collection of conditions in which platelet function is compromised. Genetic variants at multiple loci have been associated with platelet-type bleeding disorders. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple platelet-type bleeding disorder-associated loci simultaneously.
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