APA (7th ed.) Citation

S, H., S, K., H, Q., A, A., S, F., S, S., . . . I, A. (2026). Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2. Pediatric nephrology (Berlin, Germany), 41(7), 2033. https://doi.org/10.1007/s00467-026-07203-y

Chicago Style (17th ed.) Citation

S, Hashmi, et al. "Clinical Burden, Genetic Heterogeneity, and Diagnostic Implications in Primary Hyperoxaluria Type 2." Pediatric Nephrology (Berlin, Germany) 41, no. 7 (2026): 2033. https://doi.org/10.1007/s00467-026-07203-y.

MLA (9th ed.) Citation

S, Hashmi, et al. "Clinical Burden, Genetic Heterogeneity, and Diagnostic Implications in Primary Hyperoxaluria Type 2." Pediatric Nephrology (Berlin, Germany), vol. 41, no. 7, 2026, p. 2033, https://doi.org/10.1007/s00467-026-07203-y.