Associated Papers
A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene.
Mansory EM et al.
Research and Practice in Thrombosis and Haemostasis, 2021
Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis.
Preisler B et al.
Journal of Clinical Medicine, 2021
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