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  • Molecular assay reagents intended to identify mutations in the galactosidase, alpha (GLA) gene, located at chromosome Xq22, which encodes for the enzyme alpha-galactosidase active in lysosomes. Mutations at this locus have been identified in male patients with diffuse angiokeratoderma (Fabry\'s disease), caused by alpha-galactosidase A deficiency.
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