APA (7th ed.) Citation

Ferrari, S., Regazzo, D., Omenetto, E., Scaroni, C., Semenzato, G., Fabris, F., & Vianello, F. (2021). A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome. Aging clinical and experimental research, 33(7), 1987-1992. https://doi.org/10.1007/s40520-020-01709-7

Chicago Style (17th ed.) Citation

Ferrari, Silvia, Daniela Regazzo, Elisabetta Omenetto, Carla Scaroni, Gianpietro Semenzato, Fabrizio Fabris, and Fabrizio Vianello. "A Novel RUNX1 Mutation with ANKRD26 Dysregulation Is Related to Thrombocytopenia in a Sporadic Form of Myelodysplastic Syndrome." Aging Clinical and Experimental Research 33, no. 7 (2021): 1987-1992. https://doi.org/10.1007/s40520-020-01709-7.

MLA (9th ed.) Citation

Ferrari, Silvia, et al. "A Novel RUNX1 Mutation with ANKRD26 Dysregulation Is Related to Thrombocytopenia in a Sporadic Form of Myelodysplastic Syndrome." Aging Clinical and Experimental Research, vol. 33, no. 7, 2021, pp. 1987-1992, https://doi.org/10.1007/s40520-020-01709-7.