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Molecular assay reagents intended to identify genetic variants associated with albinism, a genetic disorder characterized by reduced production of melanin in the hair, skin, or eyes. Genetic variants at multiple loci have been associated with albinism. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple albinism-associated loci simultaneously.
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