Mitochondrial complex III deficiency, nuclear type 10

Any mitochondrial complex deficiency in which the cause of the disease is a mutation in the UQCRFS1 gene.

Also known as: MC3DN10, MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency, nuclear type 10 itself.