EN-RBD


	References

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2	Peyvandi F, Duga S, Akhavan S, Mannucci PM. Rare coagulation deficiencies. Haemophilia 2002; 8: 308-321
3	Tuddenham EGD, Cooper DN. The Molecular Genetics of Haemostasis and Its Inherited Disorders. Oxford, United Kingdom: Oxford Medical Publications; 1994. Oxford Monography on Medical Genetics No. 25
4	Nichols WC, Seligsohn U, Zivelin A, et al. Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII. Cell. 1998;93:61-70.
5	Zhang B, Cunningham MA, Nichols WC, et al. Bleeding due to disruption of a cargo-specific ER to-Golgi transport complex. Nat Genet. 2003;34:220-225.
6	Sadler JE. K for koagulation. Nature. 2004;427: 493-494.
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8	Neerman-Arbez M, Honsberger A, Antonarakis SE, Morris MA. Deletion of the fibrinogen alphachain gene (FGA) causes congenital afibrinogenemia. J Clin Invest. 1999;103:215-218.
9	Bolton-Maggs PHB, Perry DJ, Chalmers EA, et al. The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 2004;10:1-36
10	British Committee for Standards in Haematology, Blood Transfusion Task Force (J. Duguid, Chairman): O'Shaughnessy DF, Atterbury C, Bolton Maggs PHB, Murphy M, Thomas D, Yates S, Williamson LM. Guidelines for the use of fresh-frozen plasma, cryoprecipitate and cryosupernatant. Br J Haematol. 2004;126:11-28
11	Di Paola J, Nugent D, Yuong G. Current therapy for rare factor deficiencies. Haemophilia 2001; suppl.1: 16-22
12	Guide for the Assessment of Clotting Factor Concentrates for the Treatment of Hemophilia: (download PDF file) http://www.wfh.org/

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