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  • Molecular assay reagents intended to identify gene variants associated with leukoencephalopathy with vanishing white matter, a neurological disorder characterized by progressive cerebellar ataxia, spasticity, and cognitive impairment. Genetic variants at multiple loci have been associated with leukoencephalopathy with vanishing white matter. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple leukoencephalopathy with vanishing white matter-associated loci simultaneously.
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