The genetic spectrum of familial hypercholesterolemia in the central south region of China-Reference-Cited by-同舟云学术

The genetic spectrum of familial hypercholesterolemia in the central south region of China

Published:2017-03 Issue: Volume:258 Page:84-88
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Xiang Rong,Fan Liang-Liang,Lin Min-Jie,Li Jing-Jing,Shi Xiang-Yu,Jin Jie-Yuan,Liu Yu-Xing,Chen Ya-Qin,Xia Kun,Zhao Shui-Ping

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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5. Diagnosis and treatment of familial hypercholesterolaemia;Hovingh;Eur. heart J.,2013

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1. Analysis of the Correlation between FH and PCSK9 and APOB Gene Mutations in Han and Mongolian Populations of the Hulunbuir;Clinical Laboratory;2024

2. Genetic identification of familial hypercholesterolemia within whole genome sequences in 6820 newborns;Clinical Genetics;2023-11-29

3. Targeting PCSK9 to tackle cardiovascular disease;Pharmacology & Therapeutics;2023-09

4. Identification of an LDLR variant in a Chinese familial hypercholesterolemia and its relation to ROS/NLRP3-Mediated pyroptosis in hepatic cells;Journal of Geriatric Cardiology;2023-05

5. Metabolomic Approach to Screening Homozygotes in Chinese Patients with Severe Familial Hypercholesterolemia;Journal of Clinical Medicine;2023-01-06