Coexistence of Peripheral Myelin Protein 22 and Dystrophin Mutations in A Chinese Boy

来源 :The 12th Annual Asian and Oceanian Myology Center (AOMC)Scie | 被引量 : 0次 | 上传用户：wwwvv9vvcom

【摘要】

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【作者】

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Zhanjun Wang Fang Cui Dajun Chen Chuanqiang Pu Zhaohui Chen Fei Yang Xusheng Huang

【机构】

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Department of Neurology, Chinese PLA General Hospital, Beijing, China;Chinese PLA 421 Central Hospit

【出处】

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The 12th Annual Asian and Oceanian Myology Center (AOMC)Scie

【发表日期】

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2013年7期

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Introduction We present a 10-year-old Chinese boy with features of Charcot-Marie-Tooth disease ＃CMT＃ and Duchenne muscular dystrophy ＃DMD＃ caused by coexistence of duplications in peripheral myelin protein 22＃PMP22＃ and a large deletion spanning exon 50 in dystrophin＃Methods: Case report＃

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Coexistence of Peripheral Myelin Protein 22 and Dystrophin Mutations in A Chinese Boy

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