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Molecular assay reagents intended to identify gene variants associated with amyotrophic lateral sclerosis, a neurodegenerative disorder characterized by progressive loss of motor neurons leading to paralysis. Genetic variants at multiple loci have been associated with amyotrophic lateral sclerosis. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple amyotrophic lateral sclerosis-associated loci simultaneously.
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