The slow but progressive disappearance of the patients with the Pro343Ser (FX Friuli) mutation
Author:
Affiliation:
1. Department of Medicine University of Padua Medical School Padua Italy
2. Department of Medicine Padua City Hospital Padua Italy
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.16991
Reference15 articles.
1. A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred
2. Factor X Friuli Coagulation Disorder: Almost 50 Years Later
3. Abnormal Factor X (Factor X Friuli) Coagulation Disorder. The Heterozygote Population
4. Factor X Friuli Coagulation Disorder
5. Molecular defect in coagulation factor XFriuli results from a substitution of serine for proline at position 343
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