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  • Molecular assay reagents intended to identify gene variants associated with hereditary ataxias, a collection of neurodegenerative disorders associated with the progressive incoordination of gait, hand movement, eye movement, and/or speech. Genetic variants at multiple loci have been associated with hereditary ataxias. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple hereditary ataxia-associated loci simultaneously.
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