Novel compound heterozygous mutations in low density lipoprotein receptor gene causes a severe phenotype in a Chinese hypercholesterolemia family-Reference-Cited by-同舟云学术

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Novel compound heterozygous mutations in low density lipoprotein receptor gene causes a severe phenotype in a Chinese hypercholesterolemia family

Published:2018-05-23 Issue: Volume: Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Cheng Xinyao¹,Huang Yifang²,Qiu Xueping²,Cheng Xiaohuan²,Jin Yalei³,Hu Yafei⁴,Yang Bing⁴,Zhao Jingbo⁴,Lei Yuhua⁴,Zheng Fang²

Affiliation:

1. Cardiovascular Division, Zhongnan Hospital, Wuhan University, Wuhan, Hubei 430071, P.R. China

2. Center for Gene Diagnosis, Zhongnan Hospital, Wuhan University, Wuhan, Hubei 430071, P.R. China

3. Geriatrics Division, Zhongnan Hospital, Wuhan University, Wuhan, Hubei 430071, P.R. China

4. Ultrasonography Division, Enshi Center Hospital, Enshi, Hubei 445000, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prevalence of genetically defined familial hypercholesterolemia and the impact on acute myocardial infarction in Taiwanese population: A hospital-based study;Frontiers in Cardiovascular Medicine;2022-09-12

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