APA (7th ed.) Citation

L, K., R, J., P, Z., W, N., SK, E., A, S., . . . K, B. (2024). A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes. HemaSphere, 8(1), e31. https://doi.org/10.1002/hem3.31

Chicago Style (17th ed.) Citation

L, Kager, et al. "A Single-center Cohort Study of Patients with Hereditary Spherocytosis in Central Europe Reveals a High Frequency of Novel Disease-causing Genotypes." HemaSphere 8, no. 1 (2024): e31. https://doi.org/10.1002/hem3.31.

MLA (9th ed.) Citation

L, Kager, et al. "A Single-center Cohort Study of Patients with Hereditary Spherocytosis in Central Europe Reveals a High Frequency of Novel Disease-causing Genotypes." HemaSphere, vol. 8, no. 1, 2024, p. e31, https://doi.org/10.1002/hem3.31.