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Propionic, methylmalonic and isovaleric acidurias are inborn errors of metabolism characterized by the accumulation of the respective organic acids due to a deficiency of the enzymes propionyl coenzyme A carboxylase, methylmalonyl coenzyme A mutase or isovaleryl coenzyme A dehydrogenase, respectively
doi: 10.1016/j.annonc.2020.11.011
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28 In this study, subjects treated with a GLP-1/GIP agonist had a larger decrease in hemoglobin A1c compared to those treated with a SGLT2 inhibitor
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