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Molecular assay reagents intended to identify gene variants associated with Ehlers-Danlos syndrome, a connective tissue disorder caused by defects in fibrillar collagen. Genetic variants at multiple loci have been associated with various forms of Ehlers-Danlos syndrome (e.g., classical, hypermobility, vascular). These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Ehlers-Danlos syndrome-associated loci simultaneously.
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