| A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review | |
| Wang, Chenglin; Li, Xinyuan; Zhou, Chunkui; Cui, Li; Zhu, Lijun; Du, Heqian; Liu, Jing; Fang, Shaokuan | |
| 刊名 | MEDICINE
 |
| 2018 | |
| 卷号 | 97期号:36 |
| 关键词 | CACNA1G cerebellar atrophy hot cross bun sign SCA42 spinocerebellar ataxia |
| ISSN号 | 0025-7974 |
| 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/3538061 |
| 专题 | 吉林大学白求恩第一医院 |
| 推荐引用方式 GB/T 7714 | Wang, Chenglin,Li, Xinyuan,Zhou, Chunkui,et al. A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review[J]. MEDICINE,2018,97(36). |
| APA | Wang, Chenglin.,Li, Xinyuan.,Zhou, Chunkui.,Cui, Li.,Zhu, Lijun.,...&Fang, Shaokuan.(2018).A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review.MEDICINE,97(36). |
| MLA | Wang, Chenglin,et al."A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review".MEDICINE 97.36(2018). |
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