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  • Molecular assay reagents intended to identify mutations in the spastic paraplegia 7, paraplegin (SPG7) gene, located at chromosome 16q24.3, which encodes for a subunit of the m-AAA protease that is localized to the inner mitochondrial membrane and functions as a chaperone to facilitate protein folding as well as proteolytic degradation of unfolded proteins. This inherited genetic mutation has been identified in patients with spastic paraplegia type 7 (HSP7).
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