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Query author contributions in Reactome

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Details on Person D'Eustachio, P, 2010-03-08

Class:IdInstanceEdit:538689
_displayNameD'Eustachio, P, 2010-03-08
_timestamp2010-03-08 00:20:44
author[Person:140934] D'Eustachio, Peter
dateTime2010-03-08 05:20:43
(modified)[LiteratureReference:70776] 3-Methylglutaconic aciduria type I is caused by mutations in AUH.
[LiteratureReference:70813] 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism
[LiteratureReference:70860] Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism
[LiteratureReference:70864] Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans
[LiteratureReference:76573] Fatty acid synthase, a proficient multifunctional enzyme.
[LiteratureReference:76575] Fatty acid synthesis and its regulation.
[LiteratureReference:77290] Recent developments in the investigation of inherited metabolic disorders using cultured human cells.
[Person:77291] Roe, CR
[LiteratureReference:77400] Beta-oxidation of long-chain fatty acids by human fibroblasts: evidence for a novel long-chain acyl-coenzyme A dehydrogenase.
[LiteratureReference:171064] The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein
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No pathways have been reviewed or authored by D'Eustachio, P, 2010-03-08 (538689)