Combined oxidative phosphorylation defect type 25

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the MARS2 gene.

Also known as: COXPD25, MARS2 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency caused by mutation in MARS2, combined oxidative phosphorylation deficiency type 25, combined oxidative phosphorylation deficiency 25

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 25 itself.