Origa, R., Cazzola, M., Mereu, E., Danjou, F., Barella, S., Giagu, N., . . . Swinkels, D. W. (2015). Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia. Haematologica (Roma), 100(5), e169-e171. https://doi.org/10.3324/haematol.2014.115733
Chicago-Zitierstil (17. Ausg.)Origa, R., M. Cazzola, E. Mereu, F. Danjou, S. Barella, N. Giagu, R. Galanello, und D. W. Swinkels. "Differences in the Erythropoiesis-hepcidin-iron Store Axis Between Hemoglobin H Disease and β-thalassemia Intermedia." Haematologica (Roma) 100, no. 5 (2015): e169-e171. https://doi.org/10.3324/haematol.2014.115733.
MLA-Zitierstil (9. Ausg.)Origa, R., et al. "Differences in the Erythropoiesis-hepcidin-iron Store Axis Between Hemoglobin H Disease and β-thalassemia Intermedia." Haematologica (Roma), vol. 100, no. 5, 2015, pp. e169-e171, https://doi.org/10.3324/haematol.2014.115733.