Complement factor HY402H gene polymorphism in coronary artery disease and atherosclerosis
Complement factor HY402H gene polymorphism in coronary artery disease and atherosclerosis
In a recent article in Atherosclerosis (October 2005), Zee et al. [12] reported null findings after testing the CFH Y402H gene polymorphism for association with atherothrombotic disorders and C-reactive protein levels. We undertook a case-control study on similar lines to investigate whether this gene polymorphism was associated with susceptibility and/or severity of coronary artery disease and atherosclerosis.
myocardial-infarction, coronary-artery-disease, polymorphism, coronary, gene, complement factor h, eye, risk, amd, atherosclerosis, linkage, factor-h, macular degeneration, association, disease
213-214
Goverdhan, S.V.
9ae32d5a-5c82-48a4-962d-1ed8acc3991e
Lotery, A.J.
5ecc2d2d-d0b4-468f-ad2c-df7156f8e514
Cree, A.J.
6724b71b-8828-4abb-971f-0856c2af555e
Ye, S.
73027825-861c-4bca-8ce6-67a325fa2d2c
2006
Goverdhan, S.V.
9ae32d5a-5c82-48a4-962d-1ed8acc3991e
Lotery, A.J.
5ecc2d2d-d0b4-468f-ad2c-df7156f8e514
Cree, A.J.
6724b71b-8828-4abb-971f-0856c2af555e
Ye, S.
73027825-861c-4bca-8ce6-67a325fa2d2c
Goverdhan, S.V., Lotery, A.J., Cree, A.J. and Ye, S.
(2006)
Complement factor HY402H gene polymorphism in coronary artery disease and atherosclerosis.
Atherosclerosis, 188 (1), .
(doi:10.1016/j.atherosclerosis.2006.04.013).
Abstract
In a recent article in Atherosclerosis (October 2005), Zee et al. [12] reported null findings after testing the CFH Y402H gene polymorphism for association with atherothrombotic disorders and C-reactive protein levels. We undertook a case-control study on similar lines to investigate whether this gene polymorphism was associated with susceptibility and/or severity of coronary artery disease and atherosclerosis.
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Published date: 2006
Keywords:
myocardial-infarction, coronary-artery-disease, polymorphism, coronary, gene, complement factor h, eye, risk, amd, atherosclerosis, linkage, factor-h, macular degeneration, association, disease
Organisations:
Faculty of Medicine
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Local EPrints ID: 62389
URI: http://eprints.soton.ac.uk/id/eprint/62389
ISSN: 0021-9150
PURE UUID: affa1906-366c-4bf9-89e5-683bd0ad4377
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Date deposited: 02 Sep 2008
Last modified: 16 Mar 2024 03:47
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Author:
S.V. Goverdhan
Author:
S. Ye
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