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

Autor: Yao, Kang1,2 (AUTHOR), Dai, Yuxiang1,2 (AUTHOR), Shen, Juan3 (AUTHOR), Wang, Yi4 (AUTHOR), Yang, Huanjie5 (AUTHOR), Wu, Runda1,2 (AUTHOR), Liao, Qijun3 (AUTHOR), Wu, Hongyi1,2 (AUTHOR), Fang, Xiaodong3 (AUTHOR), Shali, Shalaimaiti1,2 (AUTHOR), Xu, Lili1,2 (AUTHOR), Hao, Meng4 (AUTHOR), Lin, Chenhao4 (AUTHOR), Sun, Zhonghan4 (AUTHOR), Liu, Yilian4 (AUTHOR), Li, Mengxin4 (AUTHOR), Wang, Zhen1,2 (AUTHOR), Gao, Qiang5 (AUTHOR), Zhang, Shuning1,2 (AUTHOR), Li, Chenguang1,2 (AUTHOR)
Zdroj: National Science Review. Aug2022, Vol. 9 Issue 8, p1-4. 4p.
Databáze: Academic Search Ultimate
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