Mitochondrial complex IV deficiency, nuclear type 21

Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COXFA4 gene.

Also known as: MC4DN21, mitochondrial complex IV deficiency, nuclear type 21

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex IV deficiency, nuclear type 21 itself.