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Association between C1019T polymorphism of the connexin37 gene and coronary heart disease in patients with in-stent restenosis
Studies have shown that a C1019T polymorphism of the gene encoding the gap junction protein connexin37 is associated with coronary artery disease (CAD). The aim of the present study was to explore the association between the C1019T polymorphism in the connexin37 gene and CAD patients with in-stent r...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
D.A. Spandidos
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570167/ https://www.ncbi.nlm.nih.gov/pubmed/23403905 http://dx.doi.org/10.3892/etm.2012.852 |