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SLC01B1 Variants and Statin-Induced Myopathy -- A Genomewide Study NEJM 359:789-799, The SEARCH Collaborative Group, 2008 See this aricle in Pubmed Article Abstract We have identified common variants in SLCO1B1 that are strongly associated with an increased risk of statin-induced myopathy. Genotyping these variants may help to achieve the benefits of statin therapy more safely and effectively.

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(click to filter results - removes previous filter) acoustic neurinoma,bilateral adverse drug reaction chromosome 12 complications efficacy genotype myopathy risk factors safety statin therapy

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