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H Koyun

Caveolin-1 Polymorphisms in Coronary Artery Disease

Coronary atherosclerosis is a major cause of mortality. T29107A specific genotype of Caveolin-1 may be linked with coronary artery disease pathogenesis. Utility of this polymorphic variant as a diagnostic or prognostic marker in CAD warrants further trials on larger series.


Aim: To investigate the associations of G14713A and T29107A polymorphic variants of Caveolin-1 with coronary artery disease (CAD).

07 Sep, 2016
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e-Published: 09 Sep, 2016


Manuscripts that are Published Ahead of Print have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear in their original format and may not be copy edited or formatted in the style guide of this Journal. While accepted manuscripts are not yet assigned a volume, issue or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. The contents of the manuscript may change before it is published in its final form. Manuscripts in this section will be removed once they have been issued to a volume and issue, but will still retain the DOI and date of e-publication.

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