APA (7th ed.) Citation

Marsili, L., Mantecon, M., Arrondel, C., Barcia, G., Assouline, Z., Gribouval, O., . . . Heidet, L. (2025). Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism. Pediatric Nephrology, 40(9), 2823. https://doi.org/10.1007/s00467-025-06787-1

Chicago Style (17th ed.) Citation

Marsili, Luisa, et al. "Genome Sequencing Identifies RMND1 as a Strong Candidate Gene for Severe Prenatal Kidney Failure Mimicking Renal Tubular Dysgenesis Associated with Hyporeninism." Pediatric Nephrology 40, no. 9 (2025): 2823. https://doi.org/10.1007/s00467-025-06787-1.

MLA (9th ed.) Citation

Marsili, Luisa, et al. "Genome Sequencing Identifies RMND1 as a Strong Candidate Gene for Severe Prenatal Kidney Failure Mimicking Renal Tubular Dysgenesis Associated with Hyporeninism." Pediatric Nephrology, vol. 40, no. 9, 2025, p. 2823, https://doi.org/10.1007/s00467-025-06787-1.