MTHFR C677T Polymorphism as a Risk Factor of Neural Tube Defects in Malay: A Case Control Study
Major congenital malformations occur in about 3% of newborn. Several studies have suggested that homozygosity for the C677T methylenetetrahydrofolate reductase (MTHFR) variant is a potential risk factor for neural tube defects (NTDs). It has been hypothesized that the maternal folic acid supplementa...
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| Format: | Journal |
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Medical Journal of Malaysia, Malaysian Medical Association
2008
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| Online Access: | http://www.myjurnal.my/public/article-view.php?id=12734 |