ABCC9-related Intellectual disability Myopathy Syndrome is a K-ATP channelopathy with loss-of-function mutations in ABCC9 | |
Smeland, Marie F.; McClenaghan, Conor; Roessler, Helen I.; Savelberg, Sanne; Hansen, Geir Asmund Myge; Hjellnes, Helene; Arntzen, Kjell Arne; Mueller, Kai Ivar; Dybesland, Andreas Rosenberger; Harter, Theresa | |
刊名 | NATURE COMMUNICATIONS
![]() |
2019 | |
卷号 | 10 |
ISSN号 | 2041-1723 |
DOI | 10.1038/s41467-019-12428-7 |
URL标识 | 查看原文 |
收录类别 | SCIE |
语种 | 英语 |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/4214955 |
专题 | 武汉大学 |
推荐引用方式 GB/T 7714 | Smeland, Marie F.,McClenaghan, Conor,Roessler, Helen I.,et al. ABCC9-related Intellectual disability Myopathy Syndrome is a K-ATP channelopathy with loss-of-function mutations in ABCC9[J]. NATURE COMMUNICATIONS,2019,10. |
APA | Smeland, Marie F..,McClenaghan, Conor.,Roessler, Helen I..,Savelberg, Sanne.,Hansen, Geir Asmund Myge.,...&van Haaften, Gijs.(2019).ABCC9-related Intellectual disability Myopathy Syndrome is a K-ATP channelopathy with loss-of-function mutations in ABCC9.NATURE COMMUNICATIONS,10. |
MLA | Smeland, Marie F.,et al."ABCC9-related Intellectual disability Myopathy Syndrome is a K-ATP channelopathy with loss-of-function mutations in ABCC9".NATURE COMMUNICATIONS 10(2019). |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论