Combined oxidative phosphorylation deficiency 29

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the TXN2 gene.

Also known as: COXPD29, TXN2 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency 29, combined oxidative phosphorylation deficiency 29; COXPD29, combined oxidative phosphorylation deficiency caused by mutation in TXN2, combined oxidative phosphorylation deficiency type 29

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation deficiency 29 itself.