Clinical Features and Electron Transfer Flavoprotein Dehydrogenase Gene Mutation Analysis in 35 Chin

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

【摘要】

：

【作者】

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Jianying Xi Jiahong Lu Jie Lin Wenhua Zhu Chongbo Zhao Jun Huang Kai Qiao YIN Wang

【机构】

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Department of Neurology, Huashan Hospital, Fudan University, Shanghai, 200040, China

【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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Objective To investigate the clinical features and electron transfer flavoprotein dehydrogenase(ETFDH) gene mutations in 35 Chinese patients with lipid storage myopathy.Methods Clinical data were collected from 35 cases with lipid storage myopathy confirmed by muscle biopsy.The sequences of all 13 exons of ETFDH were analyzed.

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