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  • Molecular assay reagents intended to identify genetic variants associated with Hermansky-Pudlak syndrome, a multisystem disorder characterized by oculocutaneous albinism and bleeding disorders. Genetic variants at multiple loci have been associated with Hermansky-Pudlak syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Hermansky-Pudlak syndrome-associated loci simultaneously.
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