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腓骨肌萎缩症(Charcot-Marie-Tooth disease,CMT)是最常见的遗传性周围神经病,患病率1/2500[1],其中由间隙连接蛋白Connexin32(Cx32)基因突变引起的X-连锁显性腓骨肌萎缩症(X-linked dominant Charcot-Marie-Tooth dis-
Charcot-Marie-Tooth disease (CMT) is the most common hereditary peripheral neuropathy with a prevalence of 1/2500 [1], in which the X-linked phenotype caused by the connexin32 (Cx32) gene gap junction X-linked dominant Charcot-Marie-Tooth dis-