Study on the polymorphism of methylenetetrahydrofolate reductase C677T gene as the genetic predisposition of congenital heart disease in North Indian population
Background: The etiology of congenital heart disease (CHD) is still not known properly. The variant alleles in the methylenetetrahydrofolate reductase (MTHFR) C677T gene help in elevating the serum homocysteine level which is an independent predisposing factor for generating CHD. Aims and Objecti...
| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | English |
| Publicado: |
Manipal College of Medical Sciences, Pokhara
2022-02-01
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| Series: | Asian Journal of Medical Sciences |
| Subjects: | |
| Acceso en liña: | https://www.nepjol.info/index.php/AJMS/article/view/40766 |