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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
; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Thrombosis and Haemostasis
volume
95
issue
1
pages
195 - 198
publisher
Schattauer GmbH
external identifiers
  • wos:000234693100029
  • pmid:16543981
  • scopus:33645541660
ISSN
0340-6245
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Emergency medicine/Medicine/Surgery (013240200)
id
6b4b54e5-5643-49c7-a4fd-57e25d3bbc61 (old id 419595)
alternative location
http://www.schattauer.de/index.php?id=1165
date added to LUP
2016-04-01 15:48:53
date last changed
2021-09-22 05:06:59
@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    = {Schattauer 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},
  url          = {http://www.schattauer.de/index.php?id=1165},
  volume       = {95},
  year         = {2006},
}