Association of NFKB1, NKX2-5, GATA4 and RANKL gene polymorphisms with sporadic congenital heart disease in Greek patients
Congenital heart disease (CHD) is a group of structural defects of the heart and the great vessels, and one of the leading causes of death among infants and young adults. Several gene variants are involved in diverse mechanisms of cardiac and vessel development and could thus be considered candidate...
| Những tác giả chính: | , , , , , , |
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| Định dạng: | Bài viết |
| Ngôn ngữ: | English |
| Được phát hành: |
Sciendo
2021-07-01
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| Loạt: | Balkan Journal of Medical Genetics |
| Những chủ đề: | |
| Truy cập trực tuyến: | https://doi.org/10.2478/bjmg-2021-0014 |