Query author contributions in Reactome

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Details on Person Duran, M

Class:Id	Person:70780
_displayName	Duran, M
_timestamp	0000-00-00 00:00:00
firstname	Marinus
initial	M
surname	Duran
(author)	[LiteratureReference:70776] 3-Methylglutaconic aciduria type I is caused by mutations in AUH. [LiteratureReference:70789] Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria [LiteratureReference:70832] 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency Is caused by mutations in the HADH2 gene [LiteratureReference:390220] Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathy [LiteratureReference:3165233] Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment [LiteratureReference:9859042] Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria [LiteratureReference:9916885] Mutations in the gene encoding 3-hydroxyisobutyryl-CoA hydrolase results in progressive infantile neurodegeneration [LiteratureReference:9971126] Substrate specificity of human carnitine acetyltransferase: Implications for fatty acid and branched-chain amino acid metabolism
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No pathways have been reviewed or authored by Duran, M (70780)