Hopkins, P N <br/><br/>
Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction.  [electronic resource] 

 -  Arteriosclerosis and thrombosis : a journal of vascular biology   
 - 1137-46 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1049-8834 
<br/><br/><label>Standard No.: </label>10.1161/01.atv.11.5.1137  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age Factors<br/>Aged<br/>Apolipoprotein E2<br/>Apolipoproteins E--genetics<br/>Body Mass Index<br/>Child<br/>Child, Preschool<br/>Cholesterol, LDL--blood<br/>Cholesterol, VLDL--blood<br/>Female<br/>Genetic Linkage<br/>Heterozygote<br/>Humans<br/>Hyperlipoproteinemia Type II--blood<br/>Hyperlipoproteinemia Type III--blood<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Restriction Fragment Length<br/>Receptors, LDL--genetics<br/>Triglycerides--blood