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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 ; Svensson, P J LU ; Dahlbäck, Björn LU and Hillarp, A LU (1998) In Blood 91(6). p.1-2210
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author
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
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
2017-10-23 17:21:59
@article{913a376d-d676-4f4d-84e6-9674172343e6,
  author       = {Zöller, Bengt and Svensson, P J and Dahlbäck, Björn and Hillarp, A},
  issn         = {0006-4971},
  keyword      = {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},
}