Zeitz, C., Roger, J. E., Audo, I., Michiels, C., Sánchez-Farías, N., Varin, J., Frederiksen, H., Wilmet, B., Callebert, J., Gimenez, M.-L., Bouzidi, N., Blond, F., Guilllonneau, X., Fouquet, S., Léveillard, T., Smirnov, V., Vincent, A., Héon, E., Sahel, J.-A., … Picaud, S. (2023). Shedding light on myopia by studying complete congenital stationary night blindness. Progress in Retinal and Eye Research, 93, 101155. https://doi.org/10.1016/j.preteyeres.2022.101155

Wang, H.-H., Chen, N., & Wang, N.-K. (2022). Introduction and Discovery of Retinitis Pigmentosa. Retinitis Pigmentosa, 1–14. https://doi.org/10.1007/978-1-0716-2651-1_1

Qian, T., Gong, Q., Shen, H., Li, C., Wang, G., Xu, X., Schrauwen, I., & Wang, W. (2022). Novel variants in the RDH5 Gene in a Chinese Han family with fundus albipunctatus. BMC Ophthalmology, 22(1). https://doi.org/10.1186/s12886-022-02301-5

Kim, A. H., Liu, P.-K., Chang, Y.-H., Kang, E. Y.-C., Wang, H.-H., Chen, N., Tseng, Y.-J., Seo, G. H., Lee, H., Liu, L., Chao, A.-N., Chen, K.-J., Hwang, Y.-S., Wu, W.-C., Lai, C.-C., Tsang, S. H., Hsiao, M.-C., & Wang, N.-K. (2022). Congenital Stationary Night Blindness: Clinical and Genetic Features. International Journal of Molecular Sciences, 23(23), 14965. https://doi.org/10.3390/ijms232314965