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En trminos prcticos, esto se traduce en que volvis a caminar, entrenar o simplemente estar de pie sin ese dolor punzante que os acompaaba en cada paso
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)
It is a pentadecapeptide (15 amino acids) derived from a protective protein found naturally in human gastric juice
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