A novel congenital dysprothrombinemia leading to defective prothrombin maturation
- BAFUNNO, VALERIA
- Bury, Loredana
- Tiscia, Giovanni Luca
- Fierro, Tiziana
- Favuzzi, Giovanni
- Caliandro, Rocco
- Sessa, Francesco
- Grandone, Elvira
- MARGAGLIONE, MAURIZIO
- Gresele, Paolo
Publication date
January 2014
DOI ISSN
0049-3848 Citation count (estimate)
7Abstract
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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