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Correction

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

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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

Citation: The PLOS Genetics Staff (2015) Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction. PLoS Genet 11(3): e1005060. https://doi.org/10.1371/journal.pgen.1005060

Published: March 17, 2015

Copyright: © 2015 The PLOS Genetics Staff. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited