Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms

Authors

Yiqiao Zheng, Washington University School of Medicine in St. Louis
Chi Sun, Washington University School of Medicine in St. Louis
Xiaodong Zhang, Washington University School of Medicine in St. Louis
Philip A Ruzycki, Washington University School of Medicine in St. Louis
Shiming Chen, Washington University School of Medicine in St. Louis

Journal

Elife

Publication Date

11-14-2023

Volume

12

First Page

RP87147

Document Type

Open Access Publication

DOI

10.7554/eLife.87147

Rights and Permissions

Yiqiao Zheng, Chi Sun, Xiaodong Zhang, Philip A Ruzycki, Shiming Chen (2023) Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms eLife 12:RP87147. https://doi.org/10.7554/eLife.87147.4. © 2023, Zheng et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

Recommended Citation

Zheng, Yiqiao; Sun, Chi; Zhang, Xiaodong; Ruzycki, Philip A; and Chen, Shiming, "Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms." Elife. 12, RP87147 (2023).
https://digitalcommons.wustl.edu/oa_4/2762

Department

ICTS (Institute of Clinical and Translational Sciences)

Additional Links

Supplemental material is available for this article at publisher site.