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
(1998) In Blood 91(6). p.1-2210
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/913a376d-d676-4f4d-84e6-9674172343e6
- author
- Zöller, Bengt LU ; Svensson, P J LU ; Dahlbäck, Björn LU and Hillarp, A LU
- organization
- publishing date
- 1998-03-15
- 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
- 2021-07-19 04:00:33
@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}}, }