Query author contributions in Reactome

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Details on Person Jakobs, Cornelis

Class:Id	Person:70816
_displayName	Jakobs, Cornelis
_timestamp	2015-01-02 21:54:49
firstname	Cornelis
initial	C
modified	[InstanceEdit:5659966] D'Eustachio, Peter, 2015-01-02
surname	Jakobs
(author)	[LiteratureReference:70813] 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism [LiteratureReference:70944] Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT) [LiteratureReference:71326] Transaldolase deficiency: liver cirrhosis associated with a new inborn error in the pentose phosphate pathway. [LiteratureReference:177786] Ribose-5-phosphate isomerase deficiency: new inborn error in the pentose phosphate pathway associated with a slowly progressive leukoencephalopathy [LiteratureReference:200390] X-linked creatine transporter defect: an overview [LiteratureReference:390289] Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts [LiteratureReference:452019] Molecular basis of phenotypic variation in patients with argininemia [LiteratureReference:469689] The biochemistry, metabolism and inherited defects of the pentose phosphate pathway: a review [LiteratureReference:508571] Mutations in antiquitin in individuals with pyridoxine-dependent seizures [LiteratureReference:880003] Mutations in the D-2-hydroxyglutarate dehydrogenase gene cause D-2-hydroxyglutaric aciduria List all 16 refering instances
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No pathways have been reviewed or authored by Jakobs, Cornelis (70816)