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  • Molecular assay reagents intended to identify gene variants associated with hemorrhagic telangiectasia, a hereditary vascular disorder characterized by arteriovenous malformations (irregular connections between arteries and veins), which lead to hemorrhages. Genetic variants at multiple loci have been associated with hemorrhagic telangiectasia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple hemorrhagic telangiectasia-associated loci simultaneously.
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