| Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review | |
| Peng, Fang; Sun, Yi-Min; Quan, Chao; Wang, Jian; Wu, Jian-Jun | |
| 刊名 | ORPHANET JOURNAL OF RARE DISEASES
 |
| 2019 | |
| 卷号 | 14 |
| 关键词 | Hereditary spastic paraplegias (HSP) Spastic paraplegia 76(SPG76) CAPN1 mutations Ataxia |
| ISSN号 | 1750-1172 |
| URL标识 | 查看原文 |
| 语种 | 英语 |
| 内容类型 | 期刊论文 |
| URI标识 | http://www.corc.org.cn/handle/1471x/3594890 |
| 专题 | 复旦大学上海医学院 |
| 推荐引用方式 GB/T 7714 | Peng, Fang,Sun, Yi-Min,Quan, Chao,et al. Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review[J]. ORPHANET JOURNAL OF RARE DISEASES,2019,14. |
| APA | Peng, Fang,Sun, Yi-Min,Quan, Chao,Wang, Jian,&Wu, Jian-Jun.(2019).Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review.ORPHANET JOURNAL OF RARE DISEASES,14. |
| MLA | Peng, Fang,et al."Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review".ORPHANET JOURNAL OF RARE DISEASES 14(2019). |
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