APA

Rost S., Geisen C., Fregin A., Seifried E., Müller C. R. & Oldenburg J. (20061012). Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1. : Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Chicago

Rost Simone, Geisen Christof, Fregin Andreas, Seifried Erhard, Müller Clemens R and Oldenburg Johannes. 20061012. Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1. : Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Harvard

Rost S., Geisen C., Fregin A., Seifried E., Müller C. R. and Oldenburg J. (20061012). Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1. : Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

MLA

Rost Simone, Geisen Christof, Fregin Andreas, Seifried Erhard, Müller Clemens R and Oldenburg Johannes. Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1. : Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis. 20061012.