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Article

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians - 1 Dec 2013

Wang Benjing, Liu Minjuan, Yan Wenhua, Mao Jun, Jiang Dong, Li Hong, Chen Ying

Abstract excerpt

OBJECTIVE: To investigate the association of 12 single nucleotide polymorphisms (SNPs) in folate metabolic genes with congenital heart disease (CHD). METHODS: A total of 160 children with CHD and 188 control children were enrolled. Twelve SNPs related to folate metabolism, including CBS-C699T, DHFR-c594 + 59del19, FOLH1-T1561C, CBS-C699T, DHFR-c594 + 59del19, GSTO1-C428T, MTHFD-G878A and -G1958A, MTHFR-C677T and...

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Topics

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Share to Ferredoxin-NADP Reductase
Share to Folic Acid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Defects, Congenital

Share to Infant, Newborn

Share to Methylenetetrahydrofolate Reductase (NADPH2)

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Source

Identifiers

PMID: 23701284
DOI: 10.3109/14767058.2013.799648

Genes

MTR
DHFR
MTHFR
RFC1
CBS
FOLH1
GSTO1
MTRR
TCN2
TYMS

Variants

Provenance

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