APA (7th ed.) Citation

C, H., B, S., M, P., Y, C., C, L., N, T., . . . N, S. (2023). Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia. Hematology (Amsterdam, Netherlands), 28(1), 2187155. https://doi.org/10.1080/16078454.2023.2187155

Chicago Style (17th ed.) Citation

C, Hantaweepant, et al. "Whole Exome Sequencing and Rare Variant Association Study to Identify Genetic Modifiers, KLF1 Mutations, and a Novel Double Mutation in Thai Patients with Hemoglobin E/beta-thalassemia." Hematology (Amsterdam, Netherlands) 28, no. 1 (2023): 2187155. https://doi.org/10.1080/16078454.2023.2187155.

MLA (9th ed.) Citation

C, Hantaweepant, et al. "Whole Exome Sequencing and Rare Variant Association Study to Identify Genetic Modifiers, KLF1 Mutations, and a Novel Double Mutation in Thai Patients with Hemoglobin E/beta-thalassemia." Hematology (Amsterdam, Netherlands), vol. 28, no. 1, 2023, p. 2187155, https://doi.org/10.1080/16078454.2023.2187155.