CORC  > 中国医学科学院 北京协和医学院
A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing
Chen, Chen; Lu, Chao-Xia; Wang, Qiong; Cao, Li-Hua; Luo, Yang; Zhang, Xue
2016
卷号20期号:4页码:203-207
ISSN号1945-0265
DOI10.1089/gtmb.2015.0248
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/6382946
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
Chen, Chen,Lu, Chao-Xia,Wang, Qiong,et al. A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing[J],2016,20(4):203-207.
APA Chen, Chen,Lu, Chao-Xia,Wang, Qiong,Cao, Li-Hua,Luo, Yang,&Zhang, Xue.(2016).A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing.,20(4),203-207.
MLA Chen, Chen,et al."A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing".20.4(2016):203-207.
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