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The full clinical expression of methylmalonyl-CoA mutase deficiency is seen in the inherited methylmalonic aciduria of newborns
10.1038/s41598-021-81815-2 108 WangZ.KwanM

reported that autoxidation of LA enhanced by Fe(II)/ascorbate under physiological condition (37 C, pH 7.4) generates three main metabolites: a hydroxy-ketone possessing a trans -unsaturation (11( E )-10-OH-13-oxo-OME), a dihydroxy-ketone (11( E )-9,10-DiOH-13-oxo-OME), and an all- trans ketone (9( E ),11( E )-13-oxo-ODE)

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Savikj M, Stocks B, Sato S, Caidahl K, Krook A, Deshmukh AS, et al

P., and Booth, I
