Mitochondrial complex III deficiency nuclear type 6

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the CYC1 gene.

Also known as: CYC1 mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in CYC1, MC3DN6, mitochondrial Complex 3 deficiency, nuclear type 6, mitochondrial complex III deficiency, nuclear type 6

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 6 itself.