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  • Molecular assay reagents intended to identify mutations in the SH3 domain and tetratricopeptide repeats 2 (SH3TC2) gene, located at chromosome 5q32, which encodes the protein SH3 domain and tetratricopeptide repeat-containing protein 2. Genetic variants at this locus have been associated with Charcot-Marie-Tooth disease and mild mononeuropathy of the median nerve.
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