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Associations between maternal genotypes and metabolites implicated in congenital heart defects
BACKGROUND: The development of non-syndromic congenital heart defects (CHDs) involves a complex interplay of genetics, metabolism, and lifestyle. Previous studies have implicated maternal single nucleotide polymorphisms (SNPs) and altered metabolism in folate-related pathways as CHD risk factors. OB...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3523122/ https://ncbi.nlm.nih.gov/pubmed/23059056 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2012.09.022 |
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