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	NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome
	Xiang, Haotian[1,2]; Zhang, Ting[1,2]; Chen, Mengping[4]; Zhou, Xiaomin[1,2]; Li, Zhen[3]; Yan, Naihong[1,2]; Li, Shiguang[5]; Han, Yu[3]; Gong, Qiyong[5]; Liu, Xuyang[1,2,6]
	2012
卷号	18期号:[db:dc_citation_issue]页码:617
DOI	[db:dc_identifier_doi]
URL标识	查看原文
WOS记录号	[DB:DC_IDENTIFIER_WOSID]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3354126
专题	暨南大学
作者单位	1.[1]Sichuan Univ, W China Hosp, Translat Neurosci Ctr, Ophthalm Labs, Chengdu 610064, Peoples R China 2.[2]Sichuan Univ, W China Hosp, Translat Neurosci Ctr, Dept Ophthalmol, Chengdu, Peoples R China 3.[3]Peoples Hosp Leshan, Dept Ophthalmol, Leshan, Peoples R China 4.[4]Second Peoples Hosp Zhengzhou, Dept Ophthalmol, Zhengzhou, Peoples R China 5.[5]Sichuan Univ, W China Hosp, Dept Radiol, Chengdu 610064, Peoples R China 6.[6]Jinan Univ, Shenzhen Eye Hosp, Shenzhen, Peoples R China
推荐引用方式 GB/T 7714	Xiang, Haotian[1,2],Zhang, Ting[1,2],Chen, Mengping[4],et al. NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome[J],2012,18([db:dc_citation_issue]):617.
APA	Xiang, Haotian[1,2].,Zhang, Ting[1,2].,Chen, Mengping[4].,Zhou, Xiaomin[1,2].,Li, Zhen[3].,...&Liu, Xuyang[1,2,6].(2012).NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome.,18([db:dc_citation_issue]),617.
MLA	Xiang, Haotian[1,2],et al."NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome".18.[db:dc_citation_issue](2012):617.

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