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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)

European Review for Medical and Pharmacological Sciences 26 (7): 24432459

The only reliable way to preserve muscle mass during rapid weight loss is adequate protein intake combined with resistance training

A total cumulative histology score was determined [21,22,23,59]
