| Literature DB >> 19846852 |
Paolo Simioni1, Daniela Tormene, Giulio Tognin, Sabrina Gavasso, Cristiana Bulato, Nicholas P Iacobelli, Jonathan D Finn, Luca Spiezia, Claudia Radu, Valder R Arruda.
Abstract
We report a case of juvenile thrombophilia associated with a substitution of leucine for arginine at position 338 (R338L) in the factor IX gene (factor IX-R338L). The level of the mutant factor IX protein in plasma was normal, but the clotting activity of factor IX from the proband was approximately eight times the normal level. In vitro, recombinant factor IX-R338L had a specific activity that was 5 to 10 times as high as that in the recombinant wild-type factor IX. The R338 substitution causes a gain-of-function mutation, resulting in factor IX that is hyperfunctional. 2009 Massachusetts Medical SocietyEntities:
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Year: 2009 PMID: 19846852 DOI: 10.1056/NEJMoa0904377
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245