Reactome | Struys, EA

Schema > Person > Entries

dbId	71330
displayName	Struys, EA
firstname	Eduard A
initial	EA
modified	[InstanceEdit:5659966] D'Eustachio, Peter, 2015-01-02
publications	[LiteratureReference:880063] D-2-Hydroxyglutaric aciduria: unravelling the biochemical pathway and the genetic defect [LiteratureReference:880012] Kinetic characterization of human hydroxyacid-oxoacid transhydrogenase: relevance to D-2-hydroxyglutaric and gamma-hydroxybutyric acidurias [LiteratureReference:5659994] Transaldolase deficiency in a two-year-old boy with cirrhosis [LiteratureReference:469689] The biochemistry, metabolism and inherited defects of the pentose phosphate pathway: a review [LiteratureReference:8959720] Sedoheptulokinase deficiency due to a 57-kb deletion in cystinosis patients causes urinary accumulation of sedoheptulose: elucidation of the CARKL gene [LiteratureReference:9853642] IDH2 mutations in patients with D-2-hydroxyglutaric aciduria [LiteratureReference:177786] Ribose-5-phosphate isomerase deficiency: new inborn error in the pentose phosphate pathway associated with a slowly progressive leukoencephalopathy [LiteratureReference:71326] Transaldolase deficiency: liver cirrhosis associated with a new inborn error in the pentose phosphate pathway.
schemaClass	Person
surname	Struys

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