AMA
Ogarek I, Szczęsny-Choruz E, Drożdż D. Mutation of the NOP10 gene as a cause of steroid-resistant nephrotic syndrome coexisting with cataract, hearing loss, and enterocolitis. Pediatria Polska - Polish Journal of Paediatrics. 2025;100(2):199-202. doi:10.5114/polp.2025.152552.
APA
Ogarek, I., Szczęsny-Choruz, E., & Drożdż, D. (2025). Mutation of the NOP10 gene as a cause of steroid-resistant nephrotic syndrome coexisting with cataract, hearing loss, and enterocolitis. Pediatria Polska - Polish Journal of Paediatrics, 100(2), 199-202. https://doi.org/10.5114/polp.2025.152552
Chicago
Ogarek, Iwona, Elżbieta Szczęsny-Choruz, and Dorota Drożdż. 2025. "Mutation of the NOP10 gene as a cause of steroid-resistant nephrotic syndrome coexisting with cataract, hearing loss, and enterocolitis". Pediatria Polska - Polish Journal of Paediatrics 100 (2): 199-202. doi:10.5114/polp.2025.152552.
Harvard
Ogarek, I., Szczęsny-Choruz, E., and Drożdż, D. (2025). Mutation of the NOP10 gene as a cause of steroid-resistant nephrotic syndrome coexisting with cataract, hearing loss, and enterocolitis. Pediatria Polska - Polish Journal of Paediatrics, 100(2), pp.199-202. https://doi.org/10.5114/polp.2025.152552
MLA
Ogarek, Iwona et al. "Mutation of the NOP10 gene as a cause of steroid-resistant nephrotic syndrome coexisting with cataract, hearing loss, and enterocolitis." Pediatria Polska - Polish Journal of Paediatrics, vol. 100, no. 2, 2025, pp. 199-202. doi:10.5114/polp.2025.152552.
Vancouver
Ogarek I, Szczęsny-Choruz E, Drożdż D. Mutation of the NOP10 gene as a cause of steroid-resistant nephrotic syndrome coexisting with cataract, hearing loss, and enterocolitis. Pediatria Polska - Polish Journal of Paediatrics. 2025;100(2):199-202. doi:10.5114/polp.2025.152552.
