Enrichment of FLI1and RUNX1mutations in families with excessive bleeding and platelet dense granule secretion defects

MLA

Stockley, Jacqueline, et al. “Enrichment of FLI1and RUNX1mutations in Families with Excessive Bleeding and Platelet Dense Granule Secretion Defects.” Blood, vol. 122, no. 25, Dec. 2013, pp. 4090–93. EBSCOhost, https://doi.org/10.1182/blood-2013-06-506873.

APA

Stockley, J., Morgan, N. V., Bem, D., Lowe, G. C., Lordkipanidzé, M., Dawood, B., Simpson, M. A., Macfarlane, K., Horner, K., Leo, V. C., Talks, K., Motwani, J., Wilde, J. T., Collins, P. W., Makris, M., Watson, S. P., & Daly, M. E. (2013). Enrichment of FLI1and RUNX1mutations in families with excessive bleeding and platelet dense granule secretion defects. Blood, 122(25), 4090–4093. https://doi.org/10.1182/blood-2013-06-506873

Chicago

Stockley, Jacqueline, Neil V. Morgan, Danai Bem, Gillian C. Lowe, Marie Lordkipanidzé, Ban Dawood, Michael A. Simpson, et al. 2013. “Enrichment of FLI1and RUNX1mutations in Families with Excessive Bleeding and Platelet Dense Granule Secretion Defects.” Blood 122 (25): 4090–93. doi:10.1182/blood-2013-06-506873.