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10.1039/D0FO01435D 72
Hereditary folate malabsorption Hereditary folate malabsorption is caused by mutations in the SLC46A1 gene coding for the folate transporter PCFT and typically affects gastrointestinal folate absorption and folate transport into the brain (183)
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Losing muscle reduces your metabolic rate, accelerates plateau formation, and makes any reset period less effective because you are fighting against a slower metabolism
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