Ferrières, J <br/><br/>
Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation.  [electronic resource] 

 -  Circulation  Aug 1995 
 - 290-5 p.  digital 
<br/><br/> Publication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-7322 
<br/><br/><label>Standard No.: </label>10.1161/01.cir.92.3.290  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Apolipoproteins E--genetics<br/>Coronary Disease--complications<br/>Female<br/>Gene Deletion<br/>Heterozygote<br/>Humans<br/>Hyperlipoproteinemia Type II--complications<br/>Male<br/>Middle Aged<br/>Polymorphism, Genetic<br/>Receptors, LDL--genetics<br/>Risk Factors