Bile acid metabolism in familial dysbetalipoproteinaemia: studies in subjects with the apolipoprotein E-2/2 phenotype
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2362.1990.tb02261.x/fullpdf
Reference44 articles.
1. Type III hyperlipoproteinemia: recent insights into the genetic defect of familial dysbetalipoproteinemia;Mahley;Adv Intern Med,1984
2. Familial hyperlipoproteinemia type III. Deficiency of a specific apolipoprotein (apo E-III) in the very low density lipoproteins;Utermann;FEBS Letters,1975
3. Polymorphism of apolipoprotein E and occurrence of dysbetalipoproteinaemia in man;Utermann;Nature,1977
4. Familial dysbetalipoproteinemia. Abnormal binding of mutant apoprotein E to low density lipoprotein receptors of human fibroblasts and membranes from liver and adrenal of rats, rabbits and cows;Schneider;J Clin Invest,1981
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