Objective To report a Chinese Charcot Marie Tooth disease (CMT) family whose proband had abnormal brainstem auditory evoked potentials (BAEPs) and to study its relationship with connexin (Cx ) gene mutation.
Objective To report a Chinese Charcot Marie Tooth disease (CMT) family whose proband had abnormal brainstem auditory evoked potentials (BAEPs) and to study its relationship with connexin (Cx ) gene mutation.
目的 报告一个脑干听觉诱发电位有异常改变的腓骨肌萎缩症 (Charcot- Marie- Tooth dis-ease,CMT)家系 ,并探讨与连接蛋白 (connexin ,Cx )基因突变的关系。