APA (7th ed.) Citation

Zhang, B., Zhang, D., Sun, F., Si, X., Luan, M., & He, R. (2025). Identification of ETFDH gene c. 487 + 2 T > A pathogenic variant and mechanisms for polycystic kidney in neonatal onset MADD. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-03640-4

Chicago Style (17th ed.) Citation

Zhang, Bijun, Dongyang Zhang, Feiyue Sun, Xinxin Si, Meng Luan, and Rong He. "Identification of ETFDH Gene C. 487 + 2 T > A Pathogenic Variant and Mechanisms for Polycystic Kidney in Neonatal Onset MADD." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-03640-4.

MLA (9th ed.) Citation

Zhang, Bijun, et al. "Identification of ETFDH Gene C. 487 + 2 T > A Pathogenic Variant and Mechanisms for Polycystic Kidney in Neonatal Onset MADD." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-03640-4.