伴有脑干听觉诱发电位异常的腓骨肌萎缩症发现连接蛋白32基因新突变

伴有脑干听觉诱发电位异常的腓骨肌萎缩症发现连接蛋白32基因新突变的英文翻译

基本释义

• A new mutation in the connexin 32 gene of a Chinese family with Charcot-Marie-Tooth disease associated with central conduction slowing