Associated Papers
Clinical and genetic spectrum of factor XII deficiency in the Han population of East China.
Xu F et al.
Orphanet Journal of Rare Diseases, 2024
Mechanism, Functions, and Diagnostic Relevance of FXII Activation by Foreign Surfaces.
Konrath S et al.
Hamostaseologie, 2021
Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiency.
Zhang H et al.
Hematology (amsterdam, Netherlands), 2019
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