Journal
Nature Communications
Publication Date
2019
Volume
10
Issue
1
First Page
4626
Document Type
Open Access Publication
DOI
10.1038/s41467-019-12522-w.
Rights and Permissions
Lee AS, Rusch J, Lima AC, Usmani A, Huang N, Lepamets M, Vigh-Conrad KA, Worthington RE, Mägi R, Wu X, Aston KI, Atkinson JP, Carrell DT, Hess RA, O'Bryan MK, Conrad DF. Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility. Nat Commun. 2019 Oct 11;10(1):4626. doi: 10.1038/s41467-019-12522-w. 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
Lee, Arthur S.; Rusch, Jannette; Lima, Ana C.; Usmani, Abul; Huang, Ni; Wu, Xiaobo; Atkinson, John P.; Conrad, Donald F.; and al., et, "Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility." Nature Communications. 10, 1. 4626 (2019).
https://digitalcommons.wustl.edu/open_access_pubs/8349
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