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Results 1 - 3 of 3
EC Number Application Commentary Reference
Show all pathways known for 1.5.1.8Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.8medicine autosomal recessive familial hyperlysinemia type I: combined deficiency in lysine-ketoglutarate reductase and saccharopine dehydrogenase activities, EC 1.5.1.8 and EC 1.5.1.9 392364, 392365
Show all pathways known for 1.5.1.8Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.8medicine hyperlysinemia 392362
Show all pathways known for 1.5.1.8Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.8medicine hyperlysinemia: genetic disease, deficiency of lysine-ketoglutarate reductase results in extreme elevations of serum lysine 392361, 392363
Results 1 - 3 of 3