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Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype.

Lanke, Elsa LU ; Johansson, Anna LU ; Halldén, Christer LU and Lethagen, Stefan LU (2005) In Journal of Thrombosis and Haemostasis 3(12). p.2656-2663
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Journal of Thrombosis and Haemostasis
volume
3
issue
12
pages
2656 - 2663
publisher
Federation of European Neuroscience Societies and Blackwell Publishing Ltd
external identifiers
  • wos:000233623700009
  • pmid:16359504
  • scopus:29244478621
ISSN
1538-7933
DOI
10.1111/j.1538-7836.2005.01631.x
language
English
LU publication?
yes
id
d396e960-add7-43fb-af1f-c55bf2b24771 (old id 148635)
alternative location
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16359504&dopt=Abstract
date added to LUP
2007-07-25 08:57:58
date last changed
2017-01-01 04:51:46
@article{d396e960-add7-43fb-af1f-c55bf2b24771,
  author       = {Lanke, Elsa and Johansson, Anna and Halldén, Christer and Lethagen, Stefan},
  issn         = {1538-7933},
  language     = {eng},
  number       = {12},
  pages        = {2656--2663},
  publisher    = {Federation of European Neuroscience Societies and Blackwell Publishing Ltd},
  series       = {Journal of Thrombosis and Haemostasis},
  title        = {Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype.},
  url          = {http://dx.doi.org/10.1111/j.1538-7836.2005.01631.x},
  volume       = {3},
  year         = {2005},
}