Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency
Author:
Publisher
Elsevier BV
Subject
Hematology
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4. Genetic analysis of a pedigree with hereditary coagulation factor XII deficiency;Blood Coagulation & Fibrinolysis;2021-05-10
5. Double Heterozygous Mutations (Cys247Tyr and 252delAsn) Cause Factor XII Deficiency in a Chinese Family;Hämostaseologie;2020-09-11
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