APA (7th ed.) Citation

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 Style (17th ed.) Citation

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 (9th ed.) Citation

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.