S Duga Selected Research

Afibrinogenemia (Fibrinogen Deficiency)

11/2005	The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia.
12/2001	Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.
10/2000	Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation.
02/2000	Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.

4	Afibrinogenemia (Fibrinogen Deficiency) 11/2005 - 02/2000
4	Factor V Deficiency 06/2003 - 12/2000

4	Factor V (Coagulation Factor V)IBA 06/2003 - 12/2000
2	Fibrinogen (Factor I)IBA 12/2001 - 02/2000
2	Nonsense Codon (Nonsense Mutation)IBA 12/2001 - 09/2001
1	DNA (Deoxyribonucleic Acid)IBA 11/2005
1	fibrinopeptides gammaIBA 10/2000