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TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population
Aims: TCF21 knockout mice display cardiac defects, including ventricular septal defects (VSDs). Functional rs12190287 polymorphisms located within the 3′ untranslated region (3′-UTR) of TCF21 were associated with a risk of coronary heart disease in the European and Eastern populations. However, whet...
Tallennettuna:
| Julkaisussa: | Genet Test Mol Biomarkers |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Mary Ann Liebert, Inc.
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5444416/ https://ncbi.nlm.nih.gov/pubmed/28346832 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2016.0324 |
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