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  • Molecular assay reagents intended to identify gene variants associated with primary ciliary dyskinesia, a collection of genetic conditions caused by defects in cilia and/or flagella function, which leads to a range of defects including breathing problems, recurrent respiratory infections, abnormal location of internal organs, and infertility. Genetic variants at multiple loci have been associated with primary ciliary dyskinesia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple primary ciliary dyskinesia-associated loci simultaneously.
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