Study on the FBN1 Gene Mutation Spectrum in Chinese Patients With Marfan Syndrome and Association Between Genotype and Clinical Phenotype

被引：0

作者：

Xu, Shijun ^{[1
]}

Fu, Yuwei ^{[2
]}

Sun, Hairui ^{[2
]}

Wang, Jianbin ^{[3
]}

Lan, Feng ^{[4
]}

He, Yihua ^{[2
]}

Zhang, Hongjia ^{[5
]}

机构：

[1] Beijing AnZhen Hosp, Cardiothorac Surg, Beijing, Peoples R China

[2] Beijing AnZhen Hosp, Echocardiog Dept, Beijing, Peoples R China

[3] Tsinghua Univ, Ctr Life Sci, Beijing, Peoples R China

[4] Beijing AnZhen Hosp, Beijing Inst Heart Lung & Blood Vessel Dis, Beijing, Peoples R China

[5] Beijing AnZhen Hosp, Cardiothorac Surg, Beijing, Peoples R China

来源：

关键词：

Aortic diseases; Aortic aneurysm; Gene mutations; Genetics; Genome-wide association studies (GWAS);

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A15563

引用

页数：2