| A novel missense KIT mutation causing piebaldism in one Chinese family associated with cafe-au-lait macules and intertriginous freckling | |
| Jia, Wei-Xue; Xiao, Xue-Min; Wu, Jian-Bing; Ma, Yi-Ping; Ge, Yi-Ping; Li, Qi; Mao, Qiu-Xia; Li, Cheng-Rang | |
| 2015 | |
| 卷号 | 11页码:635-638 |
| 关键词 | novel mutation KIT gene neurofibromatosis type 1 |
| ISSN号 | 1178-203X |
| DOI | 10.2147/TCRM.S75544 |
| URL标识 | 查看原文 |
| 收录类别 | SCIE ; PUBMED |
| 内容类型 | 期刊论文 |
| URI标识 | http://www.corc.org.cn/handle/1471x/6661241 |
| 专题 | 中国医学科学院 北京协和医学院 |
| 推荐引用方式 GB/T 7714 | Jia, Wei-Xue,Xiao, Xue-Min,Wu, Jian-Bing,et al. A novel missense KIT mutation causing piebaldism in one Chinese family associated with cafe-au-lait macules and intertriginous freckling[J],2015,11:635-638. |
| APA | Jia, Wei-Xue.,Xiao, Xue-Min.,Wu, Jian-Bing.,Ma, Yi-Ping.,Ge, Yi-Ping.,...&Li, Cheng-Rang.(2015).A novel missense KIT mutation causing piebaldism in one Chinese family associated with cafe-au-lait macules and intertriginous freckling.,11,635-638. |
| MLA | Jia, Wei-Xue,et al."A novel missense KIT mutation causing piebaldism in one Chinese family associated with cafe-au-lait macules and intertriginous freckling".11(2015):635-638. |
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