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Molecular assay reagents intended to identify gene variants associated with surfactant deficiency, a collection of diseases caused by deficiencies in the phospholipids that line lung tissues, leading difficulties breathing. Genetic variants at multiple loci have been associated with surfactant deficiency. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple surfactant deficiency-associated loci simultaneously.
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