Combined oxidative phosphorylation deficiency 28

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the SLC25A26 gene.

Also known as: COXPD28, SLC25A26 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation defect type 28, combined oxidative phosphorylation deficiency 28, combined oxidative phosphorylation deficiency caused by mutation in SLC25A26, combined oxidative phosphorylation deficiency type 28, neonatal severe cardiopulmonary failure due to mitochondrial methylation defect

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation deficiency 28 itself.