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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 Genetics
2019, 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, ITALY