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Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome
Ling, Chao; Sui, Ruifang; Yao, Fengxia; Wu, Zhihong; Zhang, Xue; Zhang, Shuyang
2019
卷号20期号:1页码:14
关键词Congenital cataract Nance-Horan syndrome Hereditary NHS mutation
ISSN号1471-2350
DOI10.1186/s12881-018-0725-3
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/6345188
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
Ling, Chao,Sui, Ruifang,Yao, Fengxia,et al. Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome[J],2019,20(1):14.
APA Ling, Chao,Sui, Ruifang,Yao, Fengxia,Wu, Zhihong,Zhang, Xue,&Zhang, Shuyang.(2019).Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome.,20(1),14.
MLA Ling, Chao,et al."Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome".20.1(2019):14.
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