Genetic heterogeneity in familial dysbetalipoproteinemia. The E2(lys146—-gln) variant results in a dominant mode of inheritance.-Reference-Cited by-同舟云学术

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Genetic heterogeneity in familial dysbetalipoproteinemia. The E2(lys146—-gln) variant results in a dominant mode of inheritance.

Published:1990-01 Issue:1 Volume:31 Page:45-53
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Smit M,de Knijff P,van der Kooij-Meijs E,Groenendijk C,van den Maagdenberg AM,Gevers Leuven JA,Stalenhoef AF,Stuyt PM,Frants RR,Havekes LM

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference34 articles.

1. Regulation of plasma cholesterol by lipoprotein receptors;Brown;Science.,1981

2. The familial hyperlipoproteinemias;Fredrickson,1980

3. Rapid hepatic clearance of the canine lipoproteins containing only the E apoprotein by a high affinity receptor;Sherill;J. Biol. Chem.,1980

4. Polymorphism of apolipoprotein E and occurrence of dysbeta-lipoproteinemia in man;Utermann;Nature.,1977

5. Human very low density lipoprotein apolipoprotein E isoprotein polymorphism is explained by genetic variation and posttransla-tional modification;Zannis;Biochemistry.,1981

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2. Establishing the relationship between familial dysbetalipoproteinemia and genetic variants in the APOE gene;Clinical Genetics;2022-08-22

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5. The clinical and laboratory investigation of dysbetalipoproteinemia;Critical Reviews in Clinical Laboratory Sciences;2020-04-07

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