Mitochondrial complex III deficiency nuclear type 9

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC3 gene.

Also known as: UQCC3 mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in UQCC3, MC3DN9, mitochondrial Complex 3 deficiency, nuclear type 9, mitochondrial complex III deficiency, nuclear type 9

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 9 itself.