Prothrombin deficiency is a very rare disorder caused by mutations in the F2 gene that generate hypoprothrombinemia or dysprothrombinemia and is characterized by bleeding manifestations that can vary from clinically irrelevant to life-threatening.

A novel congenital dysprothrombinemia leading to defective prothrombin maturation

BAFUNNO, VALERIA;Sessa, Francesco;Grandone, Elvira;MARGAGLIONE, MAURIZIO;
2014-01-01

Abstract

Prothrombin deficiency is a very rare disorder caused by mutations in the F2 gene that generate hypoprothrombinemia or dysprothrombinemia and is characterized by bleeding manifestations that can vary from clinically irrelevant to life-threatening.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11369/332566
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