Original language | English (US) |
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Pages (from-to) | 479 |
Number of pages | 1 |
Journal | American Journal of Human Genetics |
Volume | 94 |
Issue number | 3 |
DOIs |
|
State | Published - Mar 6 2014 |
All Science Journal Classification (ASJC) codes
- Genetics
- Genetics(clinical)
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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)). / Lohmueller, Kirk E.; Sparsø, Thomas; Li, Qibin; Andersson, Ehm; Korneliussen, Thorfinn; Albrechtsen, Anders; Banasik, Karina; Grarup, Niels; Hallgrimsdottir, Ingileif; Kiil, Kristoffer; Kilpeläinen, Tuomas O.; Krarup, Nikolaj T.; Pers, Tune H.; Sanchez, Gaston; Hu, Youna; Degiorgio, Michael; Jørgensen, Torben; Sandbæk, Annelli; Lauritzen, Torsten; Brunak, Søren; Kristiansen, Karsten; Li, Yingrui; Hansen, Torben; Wang, Jun; Nielsen, Rasmus; Pedersen, Oluf.
In: American Journal of Human Genetics, Vol. 94, No. 3, 06.03.2014, p. 479.Research output: Contribution to journal › Comment/debate › peer-review
TY - JOUR
T1 - Erratum
T2 - 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))
AU - Lohmueller, Kirk E.
AU - Sparsø, Thomas
AU - Li, Qibin
AU - Andersson, Ehm
AU - Korneliussen, Thorfinn
AU - Albrechtsen, Anders
AU - Banasik, Karina
AU - Grarup, Niels
AU - Hallgrimsdottir, Ingileif
AU - Kiil, Kristoffer
AU - Kilpeläinen, Tuomas O.
AU - Krarup, Nikolaj T.
AU - Pers, Tune H.
AU - Sanchez, Gaston
AU - Hu, Youna
AU - Degiorgio, Michael
AU - Jørgensen, Torben
AU - Sandbæk, Annelli
AU - Lauritzen, Torsten
AU - Brunak, Søren
AU - Kristiansen, Karsten
AU - Li, Yingrui
AU - Hansen, Torben
AU - Wang, Jun
AU - Nielsen, Rasmus
AU - Pedersen, Oluf
PY - 2014/3/6
Y1 - 2014/3/6
UR - http://www.scopus.com/inward/record.url?scp=84896764202&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84896764202&partnerID=8YFLogxK
U2 - 10.1016/j.ajhg.2014.02.002
DO - 10.1016/j.ajhg.2014.02.002
M3 - Comment/debate
AN - SCOPUS:84896764202
VL - 94
SP - 479
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
SN - 0002-9297
IS - 3
ER -