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  • Molecular assay reagents intended to identify gene variants associated with congenital neutropenia, a bone marrow disease that leads to reduced numbers of neutrophils resulting in increased risk of infections and hematologic malignancies. Genetic variants at multiple loci have been associated with congenital neutropenia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple congenital neutropenia-associated loci simultaneously.
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