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Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction

  • The PLOS Genetics Staff

Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction

  • The PLOS Genetics Staff
PLOS
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The affiliations for the sixteenth author are incorrect. Sekar Kathiresan is affiliated not with #9 but with #3 Center of Human Genetic Research (CHGR), Massachusetts General Hospital, Boston, Massachusetts, United States of America, #4 Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America, #5 Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, United States of America and #6 Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.

Additionally the authorship contributions are incorrect. The correct contributions are equal first-author contribution for AST and HR, and an equal last-author contribution for RP, SK and HR.

Reference

  1. 1. Thormaehlen AS, Schuberth C, Won H-H, Blattmann P, Joggerst-Thomalla B, Theiss S, et al. (2015) Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction. PLoS Genet 11(2): e1004855. pmid:25647241