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	Gene mutation and clinical analysis of nephronophthisis diagnosed using whole exome sequencing: Experience from China
	Tang, Xiaoshan; Xu, Hong; Shen, Qian; Li, Guoming; Rao, Jia; Chen, Jing; Zhai, Yihui; Miao, Qianfan
刊名	CLINICAL NEPHROLOGY
	2019
卷号	92期号:2
关键词	whole exome sequencing nephronophthisis NPHP3
ISSN号	0301-0430
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3597848
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Tang, Xiaoshan,Xu, Hong,Shen, Qian,et al. Gene mutation and clinical analysis of nephronophthisis diagnosed using whole exome sequencing: Experience from China[J]. CLINICAL NEPHROLOGY,2019,92(2).
APA	Tang, Xiaoshan.,Xu, Hong.,Shen, Qian.,Li, Guoming.,Rao, Jia.,...&Miao, Qianfan.(2019).Gene mutation and clinical analysis of nephronophthisis diagnosed using whole exome sequencing: Experience from China.CLINICAL NEPHROLOGY,92(2).
MLA	Tang, Xiaoshan,et al."Gene mutation and clinical analysis of nephronophthisis diagnosed using whole exome sequencing: Experience from China".CLINICAL NEPHROLOGY 92.2(2019).

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