Cargando…

A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation

Detalles Bibliográficos
Autores principales: Prüller, Florian, Raggam, Reinhard B, Mangge, Harald, Truschnig-Wilders, Martie, Matzhold, Eva-Maria, Weiss, Eva-Christine, Hasiba, Barbara, Summers, Kelli L, Renner, Wilfried, Siegert, Gabriele, Kostka, Heike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153880/
https://www.ncbi.nlm.nih.gov/pubmed/23957718
http://dx.doi.org/10.1111/bjh.12506
_version_ 1782333343743868928
author Prüller, Florian
Raggam, Reinhard B
Mangge, Harald
Truschnig-Wilders, Martie
Matzhold, Eva-Maria
Weiss, Eva-Christine
Hasiba, Barbara
Summers, Kelli L
Renner, Wilfried
Siegert, Gabriele
Kostka, Heike
author_facet Prüller, Florian
Raggam, Reinhard B
Mangge, Harald
Truschnig-Wilders, Martie
Matzhold, Eva-Maria
Weiss, Eva-Christine
Hasiba, Barbara
Summers, Kelli L
Renner, Wilfried
Siegert, Gabriele
Kostka, Heike
author_sort Prüller, Florian
collection PubMed
description
format Online
Article
Text
id pubmed-4153880
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-41538802014-09-08 A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation Prüller, Florian Raggam, Reinhard B Mangge, Harald Truschnig-Wilders, Martie Matzhold, Eva-Maria Weiss, Eva-Christine Hasiba, Barbara Summers, Kelli L Renner, Wilfried Siegert, Gabriele Kostka, Heike Br J Haematol Correspondence Blackwell Publishing Ltd 2013-11 2013-08-19 /pmc/articles/PMC4153880/ /pubmed/23957718 http://dx.doi.org/10.1111/bjh.12506 Text en © 2013 The Authors. British Journal of Haematology published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Correspondence
Prüller, Florian
Raggam, Reinhard B
Mangge, Harald
Truschnig-Wilders, Martie
Matzhold, Eva-Maria
Weiss, Eva-Christine
Hasiba, Barbara
Summers, Kelli L
Renner, Wilfried
Siegert, Gabriele
Kostka, Heike
A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation
title A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation
title_full A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation
title_fullStr A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation
title_full_unstemmed A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation
title_short A novel factor V mutation causes a normal activated protein C ratio despite the presence of a heterozygous F5 R506Q (factor V Leiden) mutation
title_sort novel factor v mutation causes a normal activated protein c ratio despite the presence of a heterozygous f5 r506q (factor v leiden) mutation
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153880/
https://www.ncbi.nlm.nih.gov/pubmed/23957718
http://dx.doi.org/10.1111/bjh.12506
work_keys_str_mv AT prullerflorian anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT raggamreinhardb anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT manggeharald anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT truschnigwildersmartie anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT matzholdevamaria anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT weissevachristine anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT hasibabarbara anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT summerskellil anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT rennerwilfried anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT siegertgabriele anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT kostkaheike anovelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT prullerflorian novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT raggamreinhardb novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT manggeharald novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT truschnigwildersmartie novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT matzholdevamaria novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT weissevachristine novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT hasibabarbara novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT summerskellil novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT rennerwilfried novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT siegertgabriele novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation
AT kostkaheike novelfactorvmutationcausesanormalactivatedproteincratiodespitethepresenceofaheterozygousf5r506qfactorvleidenmutation