APA (7e ed.) Bronvermelding

Viprakasit, V., Ekwattanakit, S., Riolueang, S., Chalaow, N., Fisher, C., Lower, K., . . . Higgs, D. (2014). Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression. American Society of Hematology.

Chicago (17e ed.) Bronvermelding

Viprakasit, V., et al. Mutations in Kruppel-like Factor 1 Cause Transfusion-dependent Hemolytic Anemia and Persistence of Embryonic Globin Gene Expression. American Society of Hematology, 2014.

MLA (9e ed.) Bronvermelding

Viprakasit, V., et al. Mutations in Kruppel-like Factor 1 Cause Transfusion-dependent Hemolytic Anemia and Persistence of Embryonic Globin Gene Expression. American Society of Hematology, 2014.