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	A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome
	Yin, Y.[1]; Liu, X. -H.[2]; Li, X. -H.[3]; Fan, N.[2]; Lei, D. -F.[4]; Wang, Y.[2]; Cai, S. -P.[2]; Zhou, X. -M.[3]; Chen, X. -M.[3]; Liu, X. -Y.[2]
	2015
卷号	14期号:2页码:4125
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4762509
专题	暨南大学
作者单位	1.[1]Sichuan Univ, State Key Lab Biotherapy, Chengdu 610064, Sichuan, Peoples R China 2.[2]Jinan Univ, Shenzhen Eye Hosp, Shenzhen Key Lab Ophthalmol, Shenzhen, Peoples R China 3.[3]Sichuan Univ, West China Hosp, Regenerat Med Res Ctr, Chengdu 610064, Sichuan, Peoples R China 4.[4]Univ South China, Affiliated Hosp 2, Dept Ophthalmol, Hengyang, Peoples R China
推荐引用方式 GB/T 7714	Yin, Y.[1],Liu, X. -H.[2],Li, X. -H.[3],et al. A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome[J],2015,14(2):4125.
APA	Yin, Y.[1].,Liu, X. -H.[2].,Li, X. -H.[3].,Fan, N.[2].,Lei, D. -F.[4].,...&Liu, X. -Y.[2].(2015).A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome.,14(2),4125.
MLA	Yin, Y.[1],et al."A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome".14.2(2015):4125.

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