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The residual GSH concentration in MG003 was also high (6.9 0.20 mM), which was 2.1-fold that of in E
Most genetic diseases associated with PDHc deficiency are due to mutations in either of the two subunits ( encoded by the PDHA1 gene or encoded by the PDHB gene) of the functional PDH heterotetramer of the PDHc
49 The matrix contains copper ion-ligand (CuL) complexes that provide copper ions for cytochrome c oxidase and superoxide dismutase assembly
doi: 10.2217/ijh-2017-0011
10.3389/fphar.2019.01466 125 LifeiL.ZhangJ.LiX.ZhuY.WangY.LiuD
