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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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| Päätekijät: | , , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2009
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| Aiheet: | |
| Linkit: | 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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