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doi: 10.3389/fphar.2021.671563 202

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Assessment of these studies is complicated by the use of membranes of different composition, attainment of different Kt/V levels, short study duration, and inclusion of patients not on ESA therapy

Both amino acids maintain potency through standard encapsulation, tableting, and powder processing methods when handled according to established protocols

Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)