HIGHLIGHTS
- who: Natau0161a Karas Kuu017eeliu010dki et al. from the Department of Clinical Biochemistry, Faculty of Pharmacy, University of Ljubljana, Au0161kercu030ceva Cesta , have published the research: A Common Polymorphism in the MTHFD1 Gene Is a Modulator of Risk of Congenital Heart Disease, in the Journal: (JOURNAL)
- how: The authors investigated the association of polymorphisms in the genes of the folate and methionine pathways with CHDs using different strategies case-control mother-child pair design and family-based association study. The associations were tested for each of the single nucleotide polymorphisms with CHD (all) or with subgroups of . . .
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