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Secondary folic acid deficiency The molecular basis of the inherited folate absorption disorder is a mutation in the SLC46A1 gene, which encodes the proton-coupled folate transporter (PCFT)
Specifications Molecular Formula: C62H98N16O22 Molecular Weight: 1419.5 g/mol Purity: 99% (HPLC Verified) Format: Lyophilized White Powder Storage: Store at 20C for long-term stability
When these medications mess with B12, it can cause fatigue, weakness, and neurological issues
15 Sublingual B12 is also much more affordable than injections, and avoids the pain and cost of repeated clinic visits
Its important to monitor levels and consult with a healthcare provider before starting treatment
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