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  • Molecular assay reagents intended to identify mutations in the mitofusin 2 (MFN2) gene, located at chromosome 1p36.22, which encodes for mitofusin 2 protein, that helps determine the morphology of mitochondria. Mutations at this locus have been identified in patients with Charcot-Marie-Tooth neuropathy type 2A2 (CMT2A2).
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