Persistent URL of this record https://hdl.handle.net/1887/113907
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Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure
- All authors
- Smith, J.G.; Felix, J.F.; Morrison, A.C.; Kalogeropoulos, A.; Trompet, S.; Wilk, J.B.; Gidlof, O.; Wang, X.C.; Morley, M.; Mendelson, M.; Joehanes, R.; Ligthart, S.; Shan, X.Y.; Bis, J.C.; Wang, Y.A.; Sjogren, M.; Ngwa, J.; Brandimarto, J.; Stott, D.J.; Aguilar, D.; Rice, K.M.; Sesso, H.D.; Demissie, S.; Buckley, B.M.; Taylor, K.D.; Ford, I.; Yao, C.; Liu, C.Y.; Sotoodehnia, N.; Harst, P. van der; Stricker, B.H.C.; Kritchevsky, S.B.; Liu, Y.M.; Gaziano, J.M.; Hofman, A.; Moravec, C.S.; Uitterlinden, A.G.; Kellis, M.; Meurs, J.B. van; Margulies, K.B.; Dehghan, A.; Levy, D.; Olde, B.; Psaty, B.M.; Cupples, L.A.; Jukema, J.W.; Djousse, L.; Franco, O.H.; Boerwinkle, E.; Boyer, L.A.; Newton-Cheh, C.; Butler, J.; Vasan, R.S.; Cappola, T.P.; Smith, N.L.; CHARGE-SCD Consortium; EchoGen Consortium; QT-IGC Consortium; CHARGE-QRS Consortium
- Date
- 2016-05-31
- Journal
- PLoS Genetics
- Volume
- 12
- Issue
- 5