Identification of loci conferring risk for premature CAD and heterozygous familial hyperlipidemia in the LDLR, APOB and PCSK9 genes
Author:
Publisher
Elsevier BV
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference52 articles.
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Cited by 3 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. Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels;PLOS ONE;2019-05-31
2. Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs*33)) causing familial hypercholesterolemia in Saudi Arab homozygous children;Genomics;2016-01
3. Familial hypercholesterolemia mutations in the Middle Eastern and North African region: A need for a national registry;Journal of Clinical Lipidology;2015-03
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