APA (7th ed.) Citation

Esson, G., Logan, I., Wood, K., Browning, A. C., & Sayer, J. A. (2024). Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure. Journal of Rare Diseases, 3(1), . https://doi.org/10.1007/s44162-024-00031-4

Chicago Style (17th ed.) Citation

Esson, Gavin, Ian Logan, Katrina Wood, Andrew C. Browning, and John A. Sayer. "Diverse Retinal-kidney Phenotypes Associated with NPHP1 Homozygous Whole-gene Deletions in Patients with Kidney Failure." Journal of Rare Diseases 3, no. 1 (2024). https://doi.org/10.1007/s44162-024-00031-4.

MLA (9th ed.) Citation

Esson, Gavin, et al. "Diverse Retinal-kidney Phenotypes Associated with NPHP1 Homozygous Whole-gene Deletions in Patients with Kidney Failure." Journal of Rare Diseases, vol. 3, no. 1, 2024, https://doi.org/10.1007/s44162-024-00031-4.