Bertamino, M., Goldberg, D. J., Mughal, M. Z., Pabst, L., Liao, Y. J., Sun, L. R., . . . Ziegler, S. G. (2025). Pediatric ABCC6 deficiency: A genotypic and phenotypic analysis. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-04102-7
Chicago Style (17th ed.) CitationBertamino, Marta, et al. "Pediatric ABCC6 Deficiency: A Genotypic and Phenotypic Analysis." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-04102-7.
MLA (9th ed.) CitationBertamino, Marta, et al. "Pediatric ABCC6 Deficiency: A Genotypic and Phenotypic Analysis." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-04102-7.
Warning: These citations may not always be 100% accurate.