Futema, Marta <br/><br/>
Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries.  [electronic resource] 

 -  Clinical chemistry  Jan 2015 
 - 231-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1530-8561 
<br/><br/><label>Standard No.: </label>10.1373/clinchem.2014.231365  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alleles<br/>Apolipoproteins B--genetics<br/>Canada<br/>Case-Control Studies<br/>Child<br/>Cholesterol, LDL--blood<br/>Cohort Studies<br/>Europe<br/>Female<br/>Humans<br/>Hyperlipoproteinemia Type II--blood<br/>Israel<br/>Male<br/>Middle Aged<br/>Multifactorial Inheritance--genetics<br/>Mutation<br/>Polymorphism, Single Nucleotide<br/>Proprotein Convertase 9<br/>Proprotein Convertases--genetics<br/>ROC Curve<br/>Receptors, LDL--genetics<br/>Risk Factors<br/>Serine Endopeptidases--genetics<br/>Young Adult