Are polymorphisms in MTRR A66G and MTHFR C677T genes associated with congenital heart diseases in Iranian population?

BACKGROUND: The 5, 10-methyleneterahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) are two essential enzymes involved in folate metabolism. The relationship between genetic polymorphisms and congenital heart defects (CHDs) is inconsistent. Our aim was to investigate the associ...

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Vydáno v:Caspian J Intern Med
Hlavní autoři: Noori, Noormohammad, Miri-Moghaddam, Ebrahim, Dejkam, Asieh, Garmie, Yasman, Bazi, Ali
Médium: Artigo
Jazyk:Inglês
Vydáno: Babol University of Medical Sciences 2017
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5494041/
https://ncbi.nlm.nih.gov/pubmed/28702146
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22088/cjim.8.2.83
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