000 01656 a2200469 4500
005 20250516164028.0
264 0 _c20140113
008 201401s 0 0 eng d
022 _a1532-6535
024 7 _a10.1038/clpt.2013.161
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCarr, D F
245 0 0 _aSLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink.
_h[electronic resource]
260 _bClinical pharmacology and therapeutics
_cDec 2013
300 _a695-701 p.
_bdigital
500 _aPublication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
650 0 4 _aAged
650 0 4 _aCase-Control Studies
650 0 4 _aCreatine Kinase
_xblood
650 0 4 _aDatabases, Factual
650 0 4 _aFemale
650 0 4 _aGeneral Practice
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aHydroxymethylglutaryl-CoA Reductase Inhibitors
_xadverse effects
650 0 4 _aLiver-Specific Organic Anion Transporter 1
650 0 4 _aMale
650 0 4 _aMuscular Diseases
_xchemically induced
650 0 4 _aOrganic Anion Transporters
_xgenetics
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aUbiquinone
_xgenetics
650 0 4 _aUnited Kingdom
700 1 _aO'Meara, H
700 1 _aJorgensen, A L
700 1 _aCampbell, J
700 1 _aHobbs, M
700 1 _aMcCann, G
700 1 _avan Staa, T
700 1 _aPirmohamed, M
773 0 _tClinical pharmacology and therapeutics
_gvol. 94
_gno. 6
_gp. 695-701
856 4 0 _uhttps://doi.org/10.1038/clpt.2013.161
_zAvailable from publisher's website
999 _c23001192
_d23001192