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A novel type of mutation at the propeptide cleavage site (AlA+1Thr) causing symptomatic protein C type II deficiency
R Dodojacek1, G Höfler, B Leschnik
1Department of Paediatrics, and Ludwig Boltzmann Research Institute for Paediatric Haemostasis and Thrombosis, University of Graz, Austria.
Thrombosis Research
|October 29, 2000
Abstract
No abstract available in PubMed .
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