Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia
Journal
Genes and Immunity
Publication Date
12-17-2024
Volume
26
Issue
1
First Page
22
Last Page
26
Document Type
Open Access Publication
DOI
10.1038/s41435-024-00310-6
Rights and Permissions
Lokki, A.I., Triebwasser, M., Daly, E. et al. Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. Genes Immun 26, 22–26 (2025). https://doi.org/10.1038/s41435-024-00310-6 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
Recommended Citation
Lokki, A Inkeri; Triebwasser, Michael; Daly, Emma; FINNPEC Core Investigator Group; Kurki, Mitja I; Perola, Markus; Auro, Kirsi; Salmon, Jane E; Anuja, Java; Daly, Mark; Atkinson, John P; Laivuori, Hannele; and Meri, Seppo, "Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia." Genes and Immunity. 26, 1. 22 - 26. (2024).
https://digitalcommons.wustl.edu/oa_4/4895
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
