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Molecular assay reagents intended to identify genetic variants associated with neuronal ceroid lipofuscinoses, a genetic disorder affecting the nervous system and characterized by the accumulation of lipofuscin. Genetic variants at multiple loci have been associated with neuronal ceroid lipofuscinoses. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple neuronal ceroid lipofuscinosis-associated loci simultaneously.
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