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  • Molecular assay reagents intended to identify gene variants associated with spinocerebellar ataxias, a collection of hereditary ataxias characterized by neurodegeneration within the cerebellum and or spinal cord. Genetic variants at multiple loci have been associated with spinocerebellar ataxias. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple spinocerebellar ataxia-associated loci simultaneously.
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