Literature DB >> 25781017

Correction: systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction.

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Abstract

Entities:  

Year:  2015        PMID: 25781017      PMCID: PMC4363563          DOI: 10.1371/journal.pgen.1005060

Source DB:  PubMed          Journal:  PLoS Genet        ISSN: 1553-7390            Impact factor:   5.917


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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.
  1 in total

1.  Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction.

Authors:  Aenne S Thormaehlen; Christian Schuberth; Hong-Hee Won; Peter Blattmann; Brigitte Joggerst-Thomalla; Susanne Theiss; Rosanna Asselta; Stefano Duga; Pier Angelica Merlini; Diego Ardissino; Eric S Lander; Stacey Gabriel; Daniel J Rader; Gina M Peloso; Rainer Pepperkok; Sekar Kathiresan; Heiko Runz
Journal:  PLoS Genet       Date:  2015-02-03       Impact factor: 5.917

  1 in total

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