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CMT-Causing Gene Mutation Found in Study of Chinese Family

A novel mutation in the PMP22 gene was found in a family with Charcot-Marie-Tooth Disease (CMT) disease, and has been detailed in the study “A Novel Missense Mutation in Peripheral Myelin Protein‑22 Causes Charcot-Marie-Tooth Disease,” published in the Chinese Medical Journal. Most CMT1 patients (70-80 percent) have a…