Combined oxidative phosphorylation defect type 23

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the GTPBP3 gene.

Also known as: COXPD23, GTPBP3 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency caused by mutation in GTPBP3, combined oxidative phosphorylation deficiency type 23, combined oxidative phosphorylation deficiency 23

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 23 itself.