Familial defective apolipoprotein B-100: A review
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference69 articles.
1. In vivo evidence for reduced binding of low density lipoproteins to receptors as a cause of primary moderate hypercholesterolemia;Vega;J Clin Invest,1986
2. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding;Innerarity;Proc Natl Acad Sci U S A,1987
3. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100;Soria;Proc Natl Acad Sci U S A,1989
4. Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia;Innerarity;J Lipid Res,1990
5. Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia;Gaffney;Arterioscler Thromb Vasc Biol,1995
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