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EC Number
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Commentary
Reference
1.5.1.8
medicine
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
1.5.1.8
medicine
hyperlysinemia
392362
1.5.1.8
medicine
hyperlysinemia: genetic disease, deficiency of lysine-ketoglutarate reductase results in extreme elevations of serum lysine
392361
,
392363
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