Cite
Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B.
MLA
Kwon, M. J., et al. “Identification of Mutations in the F9 Gene Including Exon Deletion by Multiplex Ligation-Dependent Probe Amplification in 33 Unrelated Korean Patients with Haemophilia B.” Haemophilia, vol. 14, no. 5, Sept. 2008, pp. 1069–75. EBSCOhost, https://doi.org/10.1111/j.1365-2516.2008.01796.x.
APA
Kwon, M.-J., Yoo, K.-Y., Kim, H.-J., & Kim, S.-H. (2008). Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B. Haemophilia, 14(5), 1069–1075. https://doi.org/10.1111/j.1365-2516.2008.01796.x
Chicago
Kwon, M.-J., K.-Y. Yoo, H.-J. Kim, and S.-H. Kim. 2008. “Identification of Mutations in the F9 Gene Including Exon Deletion by Multiplex Ligation-Dependent Probe Amplification in 33 Unrelated Korean Patients with Haemophilia B.” Haemophilia 14 (5): 1069–75. doi:10.1111/j.1365-2516.2008.01796.x.