Ho, C K M <br/><br/>
Genetic mutations in patients with possible familial hypercholesterolaemia in South East Scotland.  [electronic resource] 

 -  Scottish medical journal  Aug 2012 
 - 148-51 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0036-9330 
<br/><br/><label>Standard No.: </label>10.1258/smj.2012.012020  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Apolipoproteins B--blood<br/>Exons--genetics<br/>Female<br/>Genetic Testing<br/>Humans<br/>Hyperlipoproteinemia Type II--diagnosis<br/>Male<br/>Mutation<br/>Phenotype<br/>Pilot Projects<br/>Receptors, LDL--blood<br/>Scotland--epidemiology<br/>Sentinel Surveillance