TY  - RPRT
TI  - Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms
AU  - Zheng, Y.
AU  - Sun, C.
AU  - Zhang, X.
AU  - Ruzycki, P.
AU  - Chen, S.
PY  - 2023
DO  - 10.1101/2023.02.01.526652
UR  - https://www.biorxiv.org/content/10.1101/2023.02.01.526652v1
ID  - 10.1101/2023.02.01.526652
ER  -