CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Association of polymorphisms near the FOXC2 gene with the risk of varicose veins in ethnic Russians
Authors
Demekhova M.
Filipenko M.
+10 more
Ilyukhin E.
Kirienko A.
Sevost’ianova K.
Shadrina A.
Shevela A.
Shonov O.
Smetanina M.
Sokolova E.
Voronina E.
Zolotukhin I.
Publication date
1 March 2020
Publisher
Abstract
© The Author(s) 2015.Objective: To investigate the association of polymorphisms located near the FOXC2 gene with the risk of varicose veins in ethnic Russians. Methods: Allele, genotype, and haplotype frequencies were determined in the sample of 474 patients with primary varicose veins and in the control group of 478 individuals without a history of chronic venous disease. Results: Polymorphisms rs7189489, rs4633732, and rs1035550 showed the association with the increased risk of varicose veins, but none of the observed associations remained significant after correction for multiple testing. Haplotype analysis revealed the association of haplotype rs7189489 C–rs4633732 T–rs34221221 C–rs1035550 C–rs34152738 T–rs12711457 G with the increased risk of varicose veins (OR = 2.67, P = 0.01). Conclusions: Our results provide evidence that the studied polymorphisms do not play a major role in susceptibility to varicose veins development in the Russian population
Similar works
Full text
Available Versions
National Open Repository Aggregator (NORA)
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:rour.neicon.ru:rour/182820
Last time updated on 04/04/2020