Conference abstract - Peer-reviewed, 2019
Rare regulatory variant in the MEF2D gene is associated with SLE in Swedish patients and contributes to the gene regulation and splicing
Kozyrev, S. V.; Farias, F. H. G.; Dahlqvist, J.; Leonard, D.; Wilbe, M.; Abramov, S. N.; Alexsson, A.; Pielberg, G. R.; Hansson-Hamlin, H.; Andersson, G.; Tandre, K.; Eloranta, M. L.; Ronnblom, L.; Lindblad-Toh, K.Published in
European Journal of Human Genetics2019, volume: 27, number: Supplement 1, pages: 207-208
Publisher: NATURE PUBLISHING GROUP
Conference
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), JUN 16-19, 2018, Milan, ITALYAuthors' information
Kozyrev, S. V.
Uppsala University
Farias, F. H. G.
Uppsala University
Farias, F. H. G.
Washington University (WUSTL)
Dahlqvist, J.
Uppsala University
Leonard, D.
Uppsala University
Swedish University of Agricultural Sciences, Department of Animal Breeding and Genetics
Uppsala University
Abramov, S. N.
Uppsala University
Abramov, S. N.
Kazan Federal University
Alexsson, A.
Uppsala University
Pielberg, G. R.
Uppsala University
Hansson-Hamlin, Helene (Hamlin, Helene)
Swedish University of Agricultural Sciences, Department of Clinical Sciences
Swedish University of Agricultural Sciences, Department of Animal Breeding and Genetics
Tandre, K.
Uppsala University
Eloranta, M. L.
Uppsala University
Ronnblom, L.
Uppsala University
Lindblad-Toh, K.
Uppsala University
Lindblad-Toh, K.
Broad Institute
UKÄ Subject classification
Medical Genetics
URI (permanent link to this page)
https://res.slu.se/id/publ/102312