Asymptomatic coinheritance of heterozygous plasminogen deficiency and the factor VLeiden mutation
McColl, M. D., Tait, R. C., Walker, I. D., McCall, F., Conkie, J. A., Perry, D. J.Volume:
8
Journal:
Blood Coagulation & Fibrinolysis
DOI:
10.1097/00001721-199704000-00007
Date:
April, 1997
File:
PDF, 345 KB
1997