MTHFR C677T polymorphism as a risk factor of neural tube defects in Malay_a case control study

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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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Bibliographic Details
Main Authors:	Hayati, AR, Zainal, AI, Tan, G.C, Ong, L.C, Khoo, T.B
Format:	Article
Language:	English
Published:	Med J Malaysia 2008
Subjects:	Q Science (General) R Medicine (General) RB Pathology
Online Access:	http://ir.unimas.my/id/eprint/2260/ 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

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