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Prüller, F; Raggam, RB; Mangge, H; Truschnig-Wilders, M; Matzhold, EM; Weiss, EC; Hasiba, B; Summers, KL; Renner, W; Siegert, G; Kostka, H.
A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation.
Br J Haematol. 2013; 163(3):414-417
Doi: 10.1111/bjh.12506
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- Führende Autor*innen der Med Uni Graz
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Prüller Florian
- Co-Autor*innen der Med Uni Graz
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Mangge Harald
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Matzhold Eva-Maria
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Raggam Reinhard Bernd
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Renner Wilfried
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Truschnig-Wilders Martini
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Weiss Eva Christine
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- Dimensions Citations:
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- Find related publications in this database (using NLM MeSH Indexing)
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Activated Protein C Resistance - genetics
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Adolescent -
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Amino Acid Substitution -
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Asymptomatic Diseases -
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Blood Coagulation Tests -
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Enzyme Activation - genetics
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Factor V - chemistry
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Factor V - genetics
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Female -
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Heterozygote -
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Humans -
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Male -
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Molecular Sequence Data -
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Mutation, Missense -
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Pedigree -
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Point Mutation -
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Protein C - analysis
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Protein Stability -
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Protein Structure, Tertiary -
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Thrombophilia - genetics
- Find related publications in this database (Keywords)
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activated protein C resistance
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activated protein C ratio
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factor V Graz
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pseudo-homozygous factor V Leiden
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pseudo-wild-type factor V Leiden