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Metabolic Pathway - Zenodo

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Last Updated: 11 February 2022

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MATERNAL GENE POLYMORPHISMS OF VITAMIN B12 METABOLIC PATHWAY AND THEIR ASSOCIATION WITH CONGENITAL HEART DISEASES

The cases and control subjects respectively were chosen as cases and control subjects respectively, 110 pregnant women with vitamin B12 deficiency and carrying fetuses with CHD and carrying fetus fetuses with CHD. An elevated risk of an offspring with CHD was found in the present study, as well as cases with GA genotype, A allele under the prevalent and allelic models respectively, and cases with AA genotype under the co-dominant and recessive models. Moreover, though Homocysteine levels in GA and AA genotypes of the CUBN G253A variant were elevated, it was discovered that all CHD case mothers were vitamin B12 deficient irrespective of the CUBN genotype.

Source link: https://zenodo.org/record/5875779

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions