2.1.1.201 | 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase deficiency |
29044765 |
A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency. |
causal interaction unassigned |
3 0 |