Bétard, C <br/><br/>
Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a 'null' LDL-receptor gene defect.  [electronic resource] 

 -  Atherosclerosis  Jan 1996 
 - 43-55 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-9150 
<br/><br/><label>Standard No.: </label>10.1016/0021-9150(95)05627-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Canada<br/>Female<br/>Gene Deletion<br/>Genetic Variation<br/>Haplotypes<br/>Heterozygote<br/>Humans<br/>Hyperlipoproteinemia Type II--genetics<br/>Male<br/>Receptors, LDL--genetics