Screening for the apolipoprotein B-100 arginine3500→ glutamine mutation in patients with type III hyperlipoproteinemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03260.x/fullpdf
Reference20 articles.
1. Apolipoprotein E-Polymorphismus, Hyperlipidämie und Herzinfarktrisiko;Assmann;Internist,1985
2. Type III hyperlipoproteinemia: diagnosis, molecular defects, pathology, and treatment;Brewer;Ann Intern Med,1983
3. Severe type III hyperlipoproteinemia in two patients maintained on chronic hemodialysis;Feussner;Klin Wochenschr,1990a
4. Type III hyperlipoproteinemia in a child with hemolytic uremic syndrome;Feussner;Metabolism,1990b
Cited by 4 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. Molecular basis of type III hyperlipoproteinemia in Germany;Human Mutation;1998
2. Genetics of type III hyperlipoproteinemia;Genetic Epidemiology;1997
3. Prevalence and association of atherosclerosis at three different arterial sites in patients with type III hyperlipoproteinemia;Atherosclerosis;1996-01
4. Interaction of the lipoprotein lipase asparagine 291–>serine mutation with body mass index determines elevated plasma triacylglycerol concentrations: a study in hyperlipidemic subjects, myocardial infarction survivors, and healthy adults.;Journal of Lipid Research;1996-01
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