Carr, D F <br/><br/>
SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink.  [electronic resource] 

 -  Clinical pharmacology and therapeutics  Dec 2013 
 - 695-701 p.  digital 
<br/><br/> Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1532-6535 
<br/><br/><label>Standard No.: </label>10.1038/clpt.2013.161  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Case-Control Studies<br/>Creatine Kinase--blood<br/>Databases, Factual<br/>Female<br/>General Practice<br/>Genotype<br/>Humans<br/>Hydroxymethylglutaryl-CoA Reductase Inhibitors--adverse effects<br/>Liver-Specific Organic Anion Transporter 1<br/>Male<br/>Muscular Diseases--chemically induced<br/>Organic Anion Transporters--genetics<br/>Polymorphism, Single Nucleotide<br/>Ubiquinone--genetics<br/>United Kingdom