Humphries, Steve E <br/><br/>
Mutational analysis in UK patients with a clinical diagnosis of familial hypercholesterolaemia: relationship with plasma lipid traits, heart disease risk and utility in relative tracing.  [electronic resource] 

 -  Journal of molecular medicine (Berlin, Germany)  Mar 2006 
 - 203-14 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0946-2716 
<br/><br/><label>Standard No.: </label>10.1007/s00109-005-0019-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cardiovascular Diseases--etiology<br/>DNA Mutational Analysis<br/>England--epidemiology<br/>Female<br/>Genetic Testing<br/>Humans<br/>Hyperlipoproteinemia Type II--complications<br/>Lipids--blood<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Prevalence<br/>Random Allocation<br/>Receptors, LDL--genetics<br/>Risk Factors