Journal
JBMR Plus
Publication Date
12-1-2022
Volume
6
Issue
12
First Page
e10692
Document Type
Open Access Publication
DOI
10.1002/jbm4.10692
Rights and Permissions
Dahir, K.M., Black, M., Gottesman, G.S., Imel, E.A., Mumm, S., Nichols, C.M. and Whyte, M.P. (2022), X-Linked Hypophosphatemia Caused by the Prevailing North American PHEX Variant c.*231A>G; Exon 13–15 Duplication Is Often Misdiagnosed as Ankylosing Spondylitis and Manifests in Both Men and Women. JBMR Plus, 6: e10692. https://doi.org/10.1002/jbm4.10692 © 2022 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Recommended Citation
Dahir, Kathryn McCrystal; Black, Margo; Gottesman, Gary S; Imel, Erik A; Mumm, Steven; Nichols, Cindy M; and Whyte, Michael P, "X-linked hypophosphatemia caused by the prevailing North American PHEX variant c.*231A>G; exon 13–15 duplication is often misdiagnosed as ankylosing spondylitis and manifests in both men and women." JBMR Plus. 6, 12. e10692 (2022).
https://digitalcommons.wustl.edu/oa_4/1571
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.