APA (7th ed.) Citation

Thormälen, A. S., Schuberth, C., Blattmann, P. N., Joggerst-Thomalla, B., Theiß, S., Pepperkok, R., & Runz, H. (2015). Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: A case for LDLR and myocardial infarction. PLoS Genetics, 11(2), . https://doi.org/10.1371/journal.pgen.1004855

Chicago Style (17th ed.) Citation

Thormälen, Aenne Solvejg, Christian Schuberth, Peter Nils Blattmann, Brigitte Joggerst-Thomalla, Susanne Theiß, Rainer Pepperkok, and Heiko Runz. "Systematic Cell-based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction." PLoS Genetics 11, no. 2 (2015). https://doi.org/10.1371/journal.pgen.1004855.

MLA (9th ed.) Citation

Thormälen, Aenne Solvejg, et al. "Systematic Cell-based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction." PLoS Genetics, vol. 11, no. 2, 2015, https://doi.org/10.1371/journal.pgen.1004855.