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Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction
Background: Elevated plasma homocysteine level is an independent risk factor for cardiovascular disease. A common mutation (nucleotid 677C‐T) in the gene coding for methylenetetrahydrofolate reductase (MTHFR) has been reported to reduce the enzymatic activity of MTHFR and is associated with elevated...
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| Publicado no: | Clin Cardiol |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Periodicals, Inc.
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6654870/ https://ncbi.nlm.nih.gov/pubmed/11303694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.4960240405 |
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