Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect

BACKGROUND: Congenital heart defect (CHD) is one of the most common birth defects in the world. The methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) genes are two of the most important candidate genes for fetal CHD. However, the correlations between the two genes...

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Detaylı Bibliyografya
Yayımlandı:Biomed Res Int
Asıl Yazarlar: Guo, Qian-nan, Wang, Hong-dan, Tie, Li-zhen, Li, Tao, Xiao, Hai, Long, Jian-gang, Liao, Shi-xiu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi 2017
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5512027/
https://ncbi.nlm.nih.gov/pubmed/28758112
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/3043476
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