发作性运动诱发性运动障碍腓骨肌萎缩症PMP22、MPZ基因突变初步分析--《2008年浙江省神经病学学术年会论文汇编》2008年 基因周围神经髓鞘蛋白22基因(peripheral myelin protein 22,PMP22)和髓鞘蛋白零基因(myelin protein zero,MPZ)突变的技术平台,对23个CMT家系先证者进行PMP22和MPZ基因突变筛查。方法:应用PCR扩增重复
Some new foundation about the research that studied the relationship between the auditory neuropathy and the auditory nerve's demyelination leaded by quiescence of MPZ gene was provided.