True congenital prothrombin deficiency due to a 'new' mutation in the pre-propeptide (ARG-39 GLN)

Acta Haematol. 2008;120(2):82-6. doi: 10.1159/000162281. Epub 2008 Oct 14.

Authors

A Girolami¹, L Santarossa, P Scarparo, N Candeo, B Girolami

Affiliation

¹ University of Padua Medical School, Department of Medical and Surgical Sciences and Northeastern Italy Association for the Study of Coagulation Disorders, Padua, Italy. [email protected]

PMID: 18852482
DOI: 10.1159/000162281

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Family Health
Female
Hemorrhage / etiology
Heterozygote
Homozygote
Humans
Hypoprothrombinemias / genetics*
Mutation*
Pregnancy
Pregnancy Outcome
Prothrombin / genetics*
Young Adult

Substances

Prothrombin