z-logo
open-access-imgOpen Access
Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese
Author(s) -
Kang Yao,
Yuxiang Dai,
Juan Shen,
Yi Wang,
Huanjie Yang,
Runda Wu,
Qijun Liao,
Hongyi Wu,
Xiaodong Fang,
Shalaimaiti Shali,
Lili Xu,
Meng Hao,
Chenhao Lin,
Zhonghan Sun,
Yilian Liu,
Mengxin Li,
Zhen Wang,
Qiang Gao,
Shuning Zhang,
Chenguang Li,
Wei Gao,
Lei Ge,
Yunzeng Zou,
Aijun Sun,
Juying Qian,
Jin Li,
Shangyu Hong,
Yan Zheng,
Junbo Ge
Publication year - 2022
Publication title -
national science review
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.433
H-Index - 54
eISSN - 2095-5138
pISSN - 2053-714X
DOI - 10.1093/nsr/nwac102
Subject(s) - exome sequencing , exome , coronary artery disease , genetics , medicine , disease , biology , mutation , cardiology , gene

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom