Factor VII deficiency: defining the clinical picture and optimizing therapeutic options

Author:

LAPECORELLA M.,MARIANI G.,

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Reference33 articles.

1. Congenital SPCA deficiency: a hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum fractions;Alexander;J Clin Invest,1951

2. Factor VII and haemostasis;Osterud;Blood Coagul Fibrinolysis,1990

3. Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation;O’Hara;Proc Natl Acad Sci U S A,1987

4. Genetic modulation of coagulation factor VII plasma levels: contribution of different polymorphisms and gender-related effects;Di Castelnuovo;Thromb Haemost,1998

5. Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma;Bernardi;Arterioscler Thromb Vasc Biol,1996

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