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

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363563/
https://www.ncbi.nlm.nih.gov/pubmed/25781017
http://dx.doi.org/10.1371/journal.pgen.1005060
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spelling pubmed-43635632015-03-23 Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction PLoS Genet Correction Public Library of Science 2015-03-17 /pmc/articles/PMC4363563/ /pubmed/25781017 http://dx.doi.org/10.1371/journal.pgen.1005060 Text en © 2015 The PLOS Genetics Staff http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Correction
Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
title Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
title_full Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
title_fullStr Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
title_full_unstemmed Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
title_short Correction: Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction
title_sort correction: systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for ldlr and myocardial infarction
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363563/
https://www.ncbi.nlm.nih.gov/pubmed/25781017
http://dx.doi.org/10.1371/journal.pgen.1005060
work_keys_str_mv AT correctionsystematiccellbasedphenotypingofmissenseallelesempowersrarevariantassociationstudiesacaseforldlrandmyocardialinfarction

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