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MTHFR Gene Variant and Folic Acid Facts Folic Acid CDC Severe hyperhomocysteinemia due to MTHFR deficiency caused by a new mutation: A case report and literature review PMC High frequency of vitamin B12 deficiency in asymptomatic individuals homozygous to MTHFR C677T mutation is associated with endothelial dysfunction and homocysteinemia American Journal of Physiology Heart and Circulatory Physiology American What To Know About MTHFR Gene Variants
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