The spectrum of rare monogenic diseases in patients with premature coronary artery disease

Author:

Teng Yaqun123,Du Tian134,Feng Siqin12,Tian Ran1,Liu Yaping5,Guo Jian1,Wang Lei1,Zhang Zhiyu12,Luan Xiaodong136,He Shan12,Zhuang Shengsheng1,Wang Yifei137,Zhang Shuyuan1,Chen Shi8,Liu Zhenyu1,Zhang Shuyang136

Affiliation:

1. Department of Cardiology, State Key Laboratory of Complex Severe and Rare disease, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China

2. Department of Internal Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China

3. Department of Basic Medical Sciences, Tsinghua University School of Medicine, Beijing 100084, China

4. Department of Breast Oncology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong 510060, China

5. McKusick-Zhang Center for Genetic Medicine, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, Beijing 100005, China

6. Tsinghua University-Peking University Joint Center for Life Sciences, Beijing 100084, China

7. Department of Cardiology, Beijing Tsinghua Changgung Hospital, Tsinghua University, Beijing 102218, China

8. Department of Endocrinology, Key Laboratory of Endocrinology of National Health Commission, Peking Union Medical College Hospital, Chinese Research Center for Behavior Medicine in Growth and Development, Beijing 100730, China

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,General Medicine

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