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Association analysis of maternal MTHFR gene polymorphisms and the occurrence of congenital heart disease in offspring
BACKGROUND: Although many studies showed that the risk of congenital heart disease (CHD) was closely related to genetic factors, the exact pathogenesis is still unknown. Our study aimed to comprehensively assess the association of single nucleotide polymorphisms (SNPs) of maternal MTHFR gene with ri...
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| Vydáno v: | BMC Cardiovasc Disord |
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| Hlavní autoři: | , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8204503/ https://ncbi.nlm.nih.gov/pubmed/34126931 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12872-021-02117-z |
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