R, D., N, S., S, W., S, P., N, N., VHW, D., . . . P, W. (2022). Assessment of iron overload in a cohort of Sri Lankan patients with transfusion dependent beta thalassaemia and its correlation with pathogenic variants in HBB, HFE, SLC40A1, and TFR2 genes. BMC pediatrics, 22(1), 344. https://doi.org/10.1186/s12887-022-03191-8
Chicago Style (17th ed.) CitationR, Dissanayake, Samarasinghe N, Waidyanatha S, Pathirana S, Neththikumara N, Dissanayake VHW, Wetthasinghe K, Gooneratne L, and Wickramasinghe P. "Assessment of Iron Overload in a Cohort of Sri Lankan Patients with Transfusion Dependent Beta Thalassaemia and Its Correlation with Pathogenic Variants in HBB, HFE, SLC40A1, and TFR2 Genes." BMC Pediatrics 22, no. 1 (2022): 344. https://doi.org/10.1186/s12887-022-03191-8.
MLA (9th ed.) CitationR, Dissanayake, et al. "Assessment of Iron Overload in a Cohort of Sri Lankan Patients with Transfusion Dependent Beta Thalassaemia and Its Correlation with Pathogenic Variants in HBB, HFE, SLC40A1, and TFR2 Genes." BMC Pediatrics, vol. 22, no. 1, 2022, p. 344, https://doi.org/10.1186/s12887-022-03191-8.