Log in to save to my catalogue

SLCO1B1 Variants and Statin-Induced Myopathy — A Genomewide Study

SLCO1B1 Variants and Statin-Induced Myopathy — A Genomewide Study

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_gup_ub_gu_se_91314

SLCO1B1 Variants and Statin-Induced Myopathy — A Genomewide Study

About this item

Full title

SLCO1B1 Variants and Statin-Induced Myopathy — A Genomewide Study

Publisher

Boston, MA: Massachusetts Medical Society

Journal title

The New England journal of medicine, 2008-08, Vol.359 (8), p.789-799

Language

English

Formats

Publication information

Publisher

Boston, MA: Massachusetts Medical Society

More information

Scope and Contents

Contents

A genomewide screen of patients with myopathy who were taking high-dose simvastatin (80 mg per day) showed a strong association between myopathy and variants of
SLCO1B1,
which encodes an organic anion–transporting polypeptide. Approximately 60% of the cases of myopathy could be attributed to these variants. The association was replicated in a...

Alternative Titles

Full title

SLCO1B1 Variants and Statin-Induced Myopathy — A Genomewide Study

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_swepub_primary_oai_gup_ub_gu_se_91314

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_gup_ub_gu_se_91314

Other Identifiers

ISSN

0028-4793,1533-4406

E-ISSN

1533-4406

DOI

10.1056/NEJMoa0801936