Associated Papers
Novel Insights into Heterozygous Factor XIII Deficiency.
Dorgalaleh A
Seminars in Thrombosis and Hemostasis, 2024
How to Assess Founder Effect in Patients with Congenital Factor XIII Deficiency.
Shahraki H et al.
International Journal of Hematology-oncology and Stem Cell Research, 2020
Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.
Ivaškevičius V et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2017
An update of the mutation profile of Factor 13 A and B genes.
Biswas A et al.
Blood Reviews, 2011
Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.
Ivaskevicius V et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2007
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