Erratum: Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086))

Kirk E. Lohmueller, Thomas Sparsø, Qibin Li, Ehm Andersson, Thorfinn Korneliussen, Anders Albrechtsen, Karina Banasik, Niels Grarup, Ingileif Hallgrimsdottir, Kristoffer Kiil, Tuomas O. Kilpeläinen, Nikolaj T. Krarup, Tune H. Pers, Gaston Sanchez, Youna Hu, Michael Degiorgio, Torben Jørgensen, Annelli Sandbæk, Torsten Lauritzen, Søren BrunakKarsten Kristiansen, Yingrui Li, Torben Hansen, Jun Wang, Rasmus Nielsen, Oluf Pedersen

Research output: Contribution to journalComment/debate

Original languageEnglish (US)
Number of pages1
JournalAmerican Journal of Human Genetics
Volume94
Issue number3
DOIs
StatePublished - Mar 6 2014

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

Cite this

Lohmueller, K. E., Sparsø, T., Li, Q., Andersson, E., Korneliussen, T., Albrechtsen, A., Banasik, K., Grarup, N., Hallgrimsdottir, I., Kiil, K., Kilpeläinen, T. O., Krarup, N. T., Pers, T. H., Sanchez, G., Hu, Y., Degiorgio, M., Jørgensen, T., Sandbæk, A., Lauritzen, T., ... Pedersen, O. (2014). Erratum: Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086)). American Journal of Human Genetics, 94(3). https://doi.org/10.1016/j.ajhg.2014.02.002