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Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency

Stanchev, H; Philips, M; Villoutreix, BO; Aksglaede, L; Lethagen, Stefan LU and Thorsen, S (2006) In Thrombosis and Haemostasis 95(1). p.195-198
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Thrombosis and Haemostasis
volume
95
issue
1
pages
195 - 198
publisher
F K Schattauer Verlag Gmbh
external identifiers
  • wos:000234693100029
  • pmid:16543981
  • scopus:33645541660
ISSN
0340-6245
language
English
LU publication?
yes
id
6b4b54e5-5643-49c7-a4fd-57e25d3bbc61 (old id 419595)
alternative location
http://www.schattauer.de/index.php?id=1165
date added to LUP
2007-10-19 12:57:38
date last changed
2019-04-02 02:36:36
@article{6b4b54e5-5643-49c7-a4fd-57e25d3bbc61,
  author       = {Stanchev, H and Philips, M and Villoutreix, BO and Aksglaede, L and Lethagen, Stefan and Thorsen, S},
  issn         = {0340-6245},
  language     = {eng},
  number       = {1},
  pages        = {195--198},
  publisher    = {F K Schattauer Verlag Gmbh},
  series       = {Thrombosis and Haemostasis},
  title        = {Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency},
  volume       = {95},
  year         = {2006},
}