Associated Papers
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Mohsenian S et al.
Blood Advances, 2024
[Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain].
Jiang LL et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2012
Identification of a novel splicing mutation in the fibrinogen Aalpha chain gene leading to hypofibrinogenaemia in a Chinese pedigree.
Chen H et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2009
Rare coagulation deficiencies.
Peyvandi F et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2002
Autosomal recessive deficiencies of coagulation factors.
Peyvandi F et al.
Reviews in Clinical and Experimental Hematology, 2001
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