Human Genome Epidemiology Literature Finder
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Query Trace: Tetralogy of Fallot and MTHFD1[original query] |
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The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects. Human mutation 2009 Feb 30 (2): 212-20. Christensen Karen E, Rohlicek Charles V, Andelfinger Gregor U, Michaud Jacques, Bigras Jean-Luc, Richter Andrea, Mackenzie Robert E, Rozen Ri |
Methylenetetrahydrofolate reductase C677T and reduced folate carrier 80 G>A polymorphisms are associated with an increased risk of conotruncal heart defects. Clinical chemistry and laboratory medicine : CCLM / FESCC 2012 Aug 50 (8): 1455-61. Gong Dingxu, Gu Haiyong, Zhang YuJian, Gong Jie, Nie Yu, Wang Jue, Zhang Hui, Liu Ruiping, Hu Shengshou, Zhang H |
MTHFR rs1801133 C>T polymorphism is associated with an increased risk of tetralogy of Fallot. Biomedical reports 2014 Mar 2 (2): 172-176. Huang Jianbing, Mei Ju, Jiang Lianyong, Jiang Zhaolei, Liu Hao, Ding Fangb |
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