Mitochondrial complex III deficiency nuclear type 3

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

Also known as: UQCRB mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in UQCRB, MC3DN3, mitochondrial Complex 3 deficiency, nuclear type 3, mitochondrial complex III deficiency, nuclear type 3

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 3 itself.