Query author contributions in Reactome

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Details on Person Mayatepek, E

Class:Id	Person:200233
_displayName	Mayatepek, E
_timestamp	2007-07-16 20:10:30
created	[InstanceEdit:200252] D'Eustachio, P, 2007-07-16 20:10:20
firstname	Ertan
initial	E
surname	Mayatepek
(author)	[LiteratureReference:200178] beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities [LiteratureReference:200268] Genetic basis of mitochondrial HMG-CoA synthase deficiency [LiteratureReference:433703] Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells [LiteratureReference:449224] Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik [LiteratureReference:8874951] Mutations in COA6 cause cytochrome c oxidase deficiency and neonatal hypertrophic cardiomyopathy [LiteratureReference:9035243] Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegeneration [LiteratureReference:9856583] Detection of 6-demethoxyubiquinone in CoQ₁₀ deficiency disorders: Insights into enzyme interactions and identification of potential therapeutics
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No pathways have been reviewed or authored by Mayatepek, E (200233)