Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
نویسنده
چکیده
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.
منابع مشابه
Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
A fundamental challenge to contemporary genetics is to distinguish rare missense alleles that disrupt protein functions from the majority of alleles neutral on protein activities. High-throughput experimental tools to securely discriminate between disruptive and non-disruptive missense alleles are currently missing. Here we establish a scalable cell-based strategy to profile the biological effe...
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عنوان ژورنال:
دوره 11 شماره
صفحات -
تاریخ انتشار 2015