Grenkowitz, Thomas <br/><br/>
Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia.  [electronic resource] 

 -  Atherosclerosis  10 2016 
 - 88-93 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1879-1484 
<br/><br/><label>Standard No.: </label>10.1016/j.atherosclerosis.2016.08.037  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alleles<br/>Apolipoproteins B--genetics<br/>Cholesterol, LDL--blood<br/>DNA Mutational Analysis<br/>Exons<br/>Female<br/>Genetic Association Studies<br/>Genetic Variation<br/>Germany<br/>Humans<br/>Hyperlipoproteinemia Type II--blood<br/>Male<br/>Middle Aged<br/>Mutation<br/>Mutation, Missense<br/>Phenotype<br/>Proprotein Convertase 9--genetics<br/>Proprotein Convertases--genetics<br/>ROC Curve<br/>Receptors, LDL--genetics<br/>Serine Endopeptidases--genetics