Associated Papers
Dysfibrinogenemia-Potential Impact of Genotype on Thrombosis or Bleeding.
Bor MV et al.
Seminars in Thrombosis and Hemostasis, 2022
Mutations Causing Mild or No Structural Damage in Interfaces of Multimerization of the Fibrinogen γ-Module More Likely Confer Negative Dominant Behaviors.
Bellacchio E
International Journal of Molecular Sciences, 2020
Fibrin(ogen) in human disease: both friend and foe.
Vilar R et al.
Haematologica, 2020
Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
Casini A et al.
Journal of Thrombosis and Haemostasis : Jth, 2017
A genetic association study of D-dimer levels with 50K SNPs from a candidate gene chip in four ethnic groups.
Weng LC et al.
Thrombosis Research, 2014
Genetic predictors of fibrin D-dimer levels in healthy adults.
Smith NL et al.
Circulation, 2011
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