MM, H., M, F., PO, F., P, d. M., & M, D. (2003). A splicing donor site point mutation in intron 6 of the plasmin inhibitor (alpha2 antiplasmin) gene with heterozygous deficiency and a bleeding tendency. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 14(1), 107. https://doi.org/10.1097/00001721-200301000-00019
Chicago Style (17th ed.) CitationMM, Hanss, Farcis M, Ffrench PO, de Mazancourt P, and Dechavanne M. "A Splicing Donor Site Point Mutation in Intron 6 of the Plasmin Inhibitor (alpha2 Antiplasmin) Gene with Heterozygous Deficiency and a Bleeding Tendency." Blood Coagulation & Fibrinolysis : An International Journal in Haemostasis and Thrombosis 14, no. 1 (2003): 107. https://doi.org/10.1097/00001721-200301000-00019.
MLA (9th ed.) CitationMM, Hanss, et al. "A Splicing Donor Site Point Mutation in Intron 6 of the Plasmin Inhibitor (alpha2 Antiplasmin) Gene with Heterozygous Deficiency and a Bleeding Tendency." Blood Coagulation & Fibrinolysis : An International Journal in Haemostasis and Thrombosis, vol. 14, no. 1, 2003, p. 107, https://doi.org/10.1097/00001721-200301000-00019.