Cite
Recurrent disease after a matched sibling hematopoietic transplant in an aplastic anemia patient with a disease risk allele, HLA-B*40:02.
MLA
Khosla, Akshita, et al. “Recurrent Disease after a Matched Sibling Hematopoietic Transplant in an Aplastic Anemia Patient with a Disease Risk Allele, HLA-B*40:02.” Blood Transfusion = Trasfusione Del Sangue, vol. 22, no. 6, Nov. 2024, pp. 525–28. EBSCOhost, https://doi.org/10.2450/BloodTransfus.674.
APA
Khosla, A., Inoue, Y., Cioccio, J., Rakszawski, K., Songdej, N., Nickolich, M., Zheng, H., Naik, S., Ehmann, C., Claxton, D., Rybka, W., Sivik, J., Mierski, J., Silar, B., Vajdic, C., Hohl, R., Shike, H., Mineishi, S., & Minagawa, K. (2024). Recurrent disease after a matched sibling hematopoietic transplant in an aplastic anemia patient with a disease risk allele, HLA-B*40:02. Blood Transfusion = Trasfusione Del Sangue, 22(6), 525–528. https://doi.org/10.2450/BloodTransfus.674
Chicago
Khosla, Akshita, Yoshitaka Inoue, Joseph Cioccio, Kevin Rakszawski, Natthapol Songdej, Myles Nickolich, Hong Zheng, et al. 2024. “Recurrent Disease after a Matched Sibling Hematopoietic Transplant in an Aplastic Anemia Patient with a Disease Risk Allele, HLA-B*40:02.” Blood Transfusion = Trasfusione Del Sangue 22 (6): 525–28. doi:10.2450/BloodTransfus.674.