Mitochondrial complex III deficiency nuclear type 7

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC2 gene.

Also known as: UQCC2 mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in UQCC2, MC3DN7, mitochondrial Complex 3 deficiency, nuclear type 7, mitochondrial complex III deficiency, nuclear type 7

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 7 itself.