Coronary Artery Disease Is Related to Methylation Disorders Caused by the c.1286A>C <i>MTHFR</i> Polymorphism and to Low Serum 5-MTHF and Folic Acid Concentrations—Preliminary Results

Background: Single nucleotide polymorphisms in gene encoding is the key enzyme in the folates pathway, methyltetrahydrofolate reductase (MTHFR), which causes methylation disorders associated with coronary artery disease (CAD). We evaluated associations between methylation disorders caused by <i&g...

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發表在:	Reports
Main Authors:	Agnieszka Pietruszyńska-Reszetarska, Robert Pietruszyński, Ireneusz Majsterek, Tomasz Popławski, Maciej Skrzypek, Beata Kolesińska, Joanna Waśko, Joanna Kapusta, Cezary Watała, Robert Irzmański
格式:	Article
語言:	英语
出版:	MDPI AG 2024-01-01
主題:	methylation 5-MTHF folic acid gene polymorphism coronary artery disease biomarker
在線閱讀:	https://www.mdpi.com/2571-841X/7/1/6