Mitochondrial complex IV deficiency, nuclear type 16

Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COX4I1 gene.

Also known as: MC4DN16, mitochondrial complex IV deficiency, nuclear type 16

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex IV deficiency, nuclear type 16 itself.