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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| Main Authors: | , , , , |
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| Format: | E-Article |
| Language: | English |
| Published: |
Med J Malaysia
2008
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| Subjects: | |
| Online Access: | http://ir.unimas.my/id/eprint/2260/1/MTHFR%20C677T%20polymorphism%20as%20a%20risk%20factor%20of%20neural%20tube%20defects%20in%20Malay_a%20case%20control%20study.pdf http://ir.unimas.my/id/eprint/2260/ |
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