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The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families

Zöller, Bengt LU orcid ; Svensson, P J LU ; Dahlbäck, Björn LU and Hillarp, A LU (1998) In Blood 91(6). p.1-2210
Please use this url to cite or link to this publication:
author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Alleles, Comorbidity, Factor V, Gene Frequency, Genetic Variation, Genotype, Humans, Protein S Deficiency, Prothrombin, Risk Factors, Sweden, Thrombophilia, Letter
in
Blood
volume
91
issue
6
pages
1 - 2210
publisher
American Society of Hematology
external identifiers
  • pmid:9490712
ISSN
0006-4971
language
English
LU publication?
yes
id
913a376d-d676-4f4d-84e6-9674172343e6
date added to LUP
2017-10-19 15:28:18
date last changed
2025-04-04 14:44:25
@article{913a376d-d676-4f4d-84e6-9674172343e6,
  author       = {{Zöller, Bengt and Svensson, P J and Dahlbäck, Björn and Hillarp, A}},
  issn         = {{0006-4971}},
  keywords     = {{Alleles; Comorbidity; Factor V; Gene Frequency; Genetic Variation; Genotype; Humans; Protein S Deficiency; Prothrombin; Risk Factors; Sweden; Thrombophilia; Letter}},
  language     = {{eng}},
  month        = {{03}},
  number       = {{6}},
  pages        = {{1--2210}},
  publisher    = {{American Society of Hematology}},
  series       = {{Blood}},
  title        = {{The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families}},
  volume       = {{91}},
  year         = {{1998}},
}