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Molecular assay reagents intended to identify gene variants associated with primary pulmonary fibrosis and Hermansky-Pudlak syndrome, a genetic disorder that leads to signs and symptoms in multiple body systems including high rates of pulmonary fibrosis. Genetic variants at multiple loci have been associated with pulmonary fibrosis and Hermansky-Pudlak syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple pulmonary fibrosis/Hermansky-Pudlak syndrome-associated loci simultaneously.
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