Associated Papers
High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.
Jadli A et al.
The Indian Journal of Medical Research, 2015
Genetic modulation of the FV(Leiden)/normal FV ratio and risk of venous thrombosis in factor V Leiden heterozygotes.
Segers O et al.
Journal of Thrombosis and Haemostasis : Jth, 2012
Inherited defects of coagulation Factor V: the thrombotic side.
Vos HL
Journal of Thrombosis and Haemostasis : Jth, 2006
Five novel mutations in the gene for human blood coagulation factor V associated with type I factor V deficiency.
van Wijk R et al.
Blood, 2001
New missense mutation in exon 13 (N789T) of the coagulation factor V gene.
Kostka H et al.
Human Mutation, 1999
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