Neřoldová, Magdaléna <br/><br/>
Rare variants in known and novel candidate genes predisposing to statin-associated myopathy.  [electronic resource] 

 -  Pharmacogenomics  08 2016 
 - 1405-14 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1744-8042 
<br/><br/><label>Standard No.: </label>10.2217/pgs-2016-0071  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Chloride Channels--genetics<br/>Exome--genetics<br/>Female<br/>Genetic Variation<br/>Genome-Wide Association Study<br/>Genotype<br/>Humans<br/>Hydroxymethylglutaryl-CoA Reductase Inhibitors--adverse effects<br/>Liver-Specific Organic Anion Transporter 1--genetics<br/>Male<br/>Middle Aged<br/>Muscular Diseases--chemically induced<br/>Rare Diseases--genetics