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Saccharomyces Cerevisiae
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Saccharopinuria
(phenotype)
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Genetic Markers
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AASS
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Most Correlated Biogroups
Saccharopine dehydrogenase, C-terminal
Alanine dehydrogenase/pyridine nucleotide transhydrogenase, NAD(H)-binding domain
Saccharopine dehydrogenase, NADP binding domain
Alanine dehydrogenase/pyridine nucleotide transhydrogenase, N-terminal
MINGUEZ_LIVER_CANCER_VASCULAR_INVASION_DN
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OMIM - Congenital disorder
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Saccharopinuria accompanied by hyperammonemia and hypercitrullinemia presented with elderly-onset ep…
Saccharopinuria (a variant form of familial hyperlysinemia)].
Saccharopinuria: a new inborn error of lysine metabolism.
Saccharopinuria].
Enzyme studies in a patient with saccharopinuria: a defect of lysine metabolism.
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