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Selected Publication:

Dodojacek, R; Höfler, G; Leschnik, B; Muntean, W.
A novel type of mutation at the propeptide cleavage site (AlA+1Thr) causing symptomatic protein C type II deficiency.
Thromb Res. 2000; 100(1):109-113 Doi: 10.1016%2FS0049-3848%2800%2900291-7 (- Case Report)
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Leading authors Med Uni Graz
Muntean Eugen
Co-authors Med Uni Graz
Höfler Gerald
Leschnik Bettina
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Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Adult -
Binding Sites - genetics
Blotting, Western - genetics
DNA Mutational Analysis - genetics
Electrophoresis, Polyacrylamide Gel - genetics
Exons - genetics
Family Health - genetics
Female - genetics
Humans - genetics
Male - genetics
Middle Aged - genetics
Point Mutation - genetics
Protein C - genetics
Protein C Deficiency - genetics
Venous Thrombosis - genetics

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