| A Novel TK2 Gene Mutation Causes Mitochondrial DNA Depletion Syndrome with Fetal Early-Onset Lipid Storage Myopathy | |
| Duoling Li; Honghao Li; Bing Wen; Jingli Shan; Kunqian Ji; Wei Li; Yuying Zhao; Tingjun Dai; Chuanzhu Yan | |
| 2013 | |
| 关键词 | DNA gene A Novel TK2 Gene Mutation Causes Mitochondrial DNA Depletion Syndrome with Fetal Early-Onset Lipid Storage Myopathy |
| 会议录 | Program & Abstracts of the 12th Annual Asian and Oceanian Myology Center (AOMC) Scientific Meeting
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| URL标识 | 查看原文 |
| 内容类型 | 会议论文 |
| URI标识 | http://www.corc.org.cn/handle/1471x/6045643 |
| 专题 | 山东大学 |
| 作者单位 | Laboratory of Neuromuscular Disorders and Departmen |
| 推荐引用方式 GB/T 7714 | Duoling Li,Honghao Li,Bing Wen,et al. A Novel TK2 Gene Mutation Causes Mitochondrial DNA Depletion Syndrome with Fetal Early-Onset Lipid Storage Myopathy[C]. 见:. |
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