Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms in Iranian ventricular septal defect subjects

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Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms in Iranian ventricular septal defect subjects

Congenital heart defects (CHD) are among the most pervasive congenital anomalies globally, occurring in an average of one in hundred living newborn babies. This occurrence of CHD is related to the relative frequency of ventricular septal defects (VSDs), which is the most common type of CHD. Heart de...

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Bibliographic Details
Main Author:	Pishva, Seyyed Reza
Format:	Thesis
Language:	English
Published:	2013
Subjects:	Amino Acid Metabolism, Inborn Errors - enzymology Methylenetetrahydrofolate Dehydrogenase (NADP) - deficiency Oxidoreductases - deficiency
Online Access:	http://psasir.upm.edu.my/id/eprint/26756/ http://psasir.upm.edu.my/id/eprint/26756/1/FPSK%28m%29%202013%207R.pdf

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