Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis | |
Lu Yan; Da Yu-Wei; Zhang Yong-Biao; Li Xin-Gang; Wang Min; Di Li; Pang Mi; Lei Lin | |
刊名 | Frontiers in neuroscience |
2018 | |
卷号 | 12页码:570 |
关键词 | CFTR hereditary inclusion body myopathy mutation next-generation sequencing whole-exome sequencing |
ISSN号 | 1662-4548 |
DOI | 10.3389/fnins.2018.00570 |
URL标识 | 查看原文 |
收录类别 | PUBMED |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/5930003 |
专题 | 北京航空航天大学 |
推荐引用方式 GB/T 7714 | Lu Yan,Da Yu-Wei,Zhang Yong-Biao,et al. Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis[J]. Frontiers in neuroscience,2018,12:570. |
APA | Lu Yan.,Da Yu-Wei.,Zhang Yong-Biao.,Li Xin-Gang.,Wang Min.,...&Lei Lin.(2018).Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis.Frontiers in neuroscience,12,570. |
MLA | Lu Yan,et al."Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis".Frontiers in neuroscience 12(2018):570. |
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