A Genetic Variant in FIGN Gene Reduces the Risk of Congenital Heart Disease in Han Chinese Populations
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DOI: 10.1007/s00246-017-1636-3
Abstract: Congenital heart disease (CHD) is one of the most common birth anomalies worldwide. Folate deficiency is an independent risk factor for CHD. Genome-wide association studies (GWAS) revealed that human folate level could be significantly influenced… read more here.
Keywords: fign gene; congenital heart; chd; fign ... See more keywords