A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts

Authors

Fabiana H G Farias, Washington University School of Medicine in St. Louis
et al

Journal

European Journal of Human Genetics

Publication Date

11-20-2018

Volume

27

Issue

3

First Page

432

Last Page

441

Document Type

Open Access Publication

DOI

10.1038/s41431-018-0297-x

Rights and Permissions

Farias, F.H.G., Dahlqvist, J., Kozyrev, S.V. et al. A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts. Eur J Hum Genet 27, 432–441 (2019). doi.org/10.1038/s41431-018-0297-x Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Recommended Citation

Farias, Fabiana H G and et al, "A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts." European Journal of Human Genetics. 27, 3. 432 - 441. (2018).
https://digitalcommons.wustl.edu/open_access_pubs/11747