Mitochondrial complex III deficiency nuclear type 1

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the BCS1L gene.

Also known as: BCS1L mitochondrial complex III deficiency, mitochondrial complex III deficiency caused by mutation in BCS1L, Complex 3 mitochondrial respiratory chain deficiency, MC3DN1, mitochondrial Complex 3 deficiency, nuclear type 1, mitochondrial complex III deficiency, mitochondrial complex III deficiency, nuclear type 1

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency nuclear type 1 itself.