A novel congenital dysprothrombinemia leading to defective prothrombin maturation

Academic Article

Publication Date:

2014

abstract:

Aim: Here we characterize a patient with a novel missense mutation in F2, c. 1090 T/A (p.Val322Glu), that causes severe dysprothrombinemia.

Iris type:

01.01 Articolo in rivista

Keywords:

Dysprothrombinemia; Factor II; Meizothrombin; Molecular modeling; Prothrombin activation

List of contributors:

Authors of the University:

CALIANDRO ROCCO

Handle:

Published in:

Journal