A Common Variant in MTHFD1L is Associated with Neural Tube Defects and mRNA Splicing Efficiency

Polymorphisms in folate-related genes have emerged as important risk factors in a range of diseases including neural tube defects (NTDs), cancer and coronary artery disease (CAD). Having previously identified a polymorphism within the cytoplasmic folate enzyme, MTHFD1, as a maternal risk factor for...

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Autori principali: Parle-McDermott, Anne, Pangilinan, Faith, O’Brien, Kirsty K., Mills, James L., Magee, Alan M., Troendle, James, Sutton, Marie, Scott, John M., Kirke, Peadar N., Molloy, Anne M., Brody, Lawrence C.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2009
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2787683/
https://ncbi.nlm.nih.gov/pubmed/19777576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21109
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