Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese

Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese

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Veröffentlicht in:National science review 2022-08, Vol.9 (8), p.nwac102-nwac102
Hauptverfasser: Yao, Kang, Dai, Yuxiang, Shen, Juan, Wang, Yi, Yang, Huanjie, Wu, Runda, Liao, Qijun, Wu, Hongyi, Fang, Xiaodong, Shali, Shalaimaiti, Xu, Lili, Hao, Meng, Lin, Chenhao, Sun, Zhonghan, Liu, Yilian, Li, Mengxin, Wang, Zhen, Gao, Qiang, Zhang, Shuning, Li, Chenguang, Gao, Wei, Ge, Lei, Zou, Yunzeng, Sun, Aijun, Qian, Juying, Jin, Li, Hong, Shangyu, Zheng, Yan, Ge, Junbo
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container_end_page nwac102
container_issue 8
container_start_page nwac102
container_title National science review
container_volume 9
creator Yao, Kang
Dai, Yuxiang
Shen, Juan
Wang, Yi
Yang, Huanjie
Wu, Runda
Liao, Qijun
Wu, Hongyi
Fang, Xiaodong
Shali, Shalaimaiti
Xu, Lili
Hao, Meng
Lin, Chenhao
Sun, Zhonghan
Liu, Yilian
Li, Mengxin
Wang, Zhen
Gao, Qiang
Zhang, Shuning
Li, Chenguang
Gao, Wei
Ge, Lei
Zou, Yunzeng
Sun, Aijun
Qian, Juying
Jin, Li
Hong, Shangyu
Zheng, Yan
Ge, Junbo
description
doi_str_mv 10.1093/nsr/nwac102
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subjects Brief Communication
title Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese
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