Xu, P., Chen, Z., Ma, J., Shan, Y., Wang, Y., Xie, B., . . . Zhong, X. (2023). Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function. Human Genetics, 142(4), 577-593. https://doi.org/10.1007/s00439-023-02531-7
Chicago-referens (17:e uppl.)Xu, Ping, et al. "Biallelic CLCN2 Mutations Cause Retinal Degeneration by Impairing Retinal Pigment Epithelium Phagocytosis and Chloride Channel Function." Human Genetics 142, no. 4 (2023): 577-593. https://doi.org/10.1007/s00439-023-02531-7.
MLA-referens (9:e uppl.)Xu, Ping, et al. "Biallelic CLCN2 Mutations Cause Retinal Degeneration by Impairing Retinal Pigment Epithelium Phagocytosis and Chloride Channel Function." Human Genetics, vol. 142, no. 4, 2023, pp. 577-593, https://doi.org/10.1007/s00439-023-02531-7.
