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not for human or veterinary application References Schneider-Helmert D., Schoenenberger G.A

FL: Conceptualization, Methodology, Writing review & editing

While severe inborn errors of folate metabolismsuch as those causing homocystinuriaare rare and typically result from deletions or deleterious mutations that abolish enzyme function, their dramatic clinical consequences have underscored the critical importance of this metabolic pathway [1-3]

In the chromatogram of the plasma-treated GSSG in the presence of complex 1 , only one peak was observed at 1.12 min, which corresponded to the GSO 3 H species