SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink.
Carr, D F
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
Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
1532-6535
10.1038/clpt.2013.161 doi
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
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
Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
1532-6535
10.1038/clpt.2013.161 doi
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