SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink. [electronic resource]
Producer: 20140113Description: 695-701 p. digitalISSN:- 1532-6535
- Aged
- Case-Control Studies
- Creatine Kinase -- blood
- Databases, Factual
- Female
- General Practice
- Genotype
- Humans
- Hydroxymethylglutaryl-CoA Reductase Inhibitors -- adverse effects
- Liver-Specific Organic Anion Transporter 1
- Male
- Muscular Diseases -- chemically induced
- Organic Anion Transporters -- genetics
- Polymorphism, Single Nucleotide
- Ubiquinone -- genetics
- United Kingdom
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Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
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