Among the Chinese CMT patients 31.9% are caused by PMP22 duplication, 6.2% by CX32, and 0.9% by HSP22, HSP27, MPZ and GDAP1. Point mutations of PMP22, EGR2 and NEFL are rare.
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释义
CMT的PMP22基因重复突变所占比例为31.;9%25;CX32基因突变所占比例为6
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