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  • Molecular assay reagents intended to identify mutations in the lamin A/C (LMNA) gene, located at chromosome 1q21.2-q21.3, which provides instructions for making several different lamin proteins. Lamin A and lamin C are made in most cells of the body. Mutations at this locus have been identified in patients with Charcot-Marie-Tooth neuropathy type 2B and Emery-Dreifuss muscular dystrophy.
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