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.

Conference abstract2019Peer reviewed

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

SLU Authors

Wilbe, Maria
- Department of Animal Biosciences, Swedish University of Agricultural Sciences
- Uppsala University
Hamlin, Helene
- Department of Clinical Sciences, Swedish University of Agricultural Sciences
Andersson, Göran
- Department of Animal Biosciences, Swedish University of Agricultural Sciences

UKÄ Subject classification

Medical Genetics and Genomics

Permanent link to this page (URI)

https://res.slu.se/id/publ/102312

Rare regulatory variant in the MEF2D gene is associated with SLE in Swedish patients and contributes to the gene regulation and splicing

Published in

Conference

SLU Authors

Wilbe, Maria

Hamlin, Helene

Andersson, Göran

UKÄ Subject classification

Permanent link to this page (URI)