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  • Molecular assay reagents intended to identify mutations in the spastin (SPAST) gene, located at chromosome 2p24-p21, which encodes for a protein that is involved many cell activities, including membrane transport, intracellular motility, organelle biogenesis, protein folding, and proteolysis. This inherited genetic mutation has been identified in patients with hereditary spastic paraplegia type 4 (SPG4).
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