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EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.1.1.201Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.2012-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
Show all pathways known for 2.1.1.201Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.201Cerebellar Ataxia 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
Results 1 - 2 of 2