Associated Papers
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient.
Platé M et al.
Biochimica Et Biophysica Acta, 2007
The molecular basis of quantitative fibrinogen disorders.
Asselta R et al.
Journal of Thrombosis and Haemostasis : Jth, 2006
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.
Asselta R et al.
Blood, 2001
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