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  • Molecular assay reagents intended to identify mutations in the calpain 3 (CAPN3) gene, located at chromosome 15q15.1-q21.1, which encodes for a muscle-specific calpain, a calcium-activated, neutral proteinase. Mutations at this locus have been identified in patients with limb-girdle muscular dystrophy type 2A (calpainopathy).
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