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Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing
AIMS: Statin-related myopathy (SRM), which includes rhabdomyolysis, is an uncommon but important adverse drug reaction because the number of people prescribed statins world-wide is large. Previous association studies of common genetic variants have had limited success in identifying a genetic basis...
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| Izdano u: | PLoS One |
|---|---|
| Glavni autori: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Public Library of Science
2019
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6594672/ https://ncbi.nlm.nih.gov/pubmed/31242253 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0218115 |
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