Query author contributions in Reactome

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Details on Person Schmidt, E

Class:Id	Person:199739
_displayName	Schmidt, E
_timestamp	2007-07-11 22:14:21
created	[InstanceEdit:199761] D'Eustachio, P, 2007-07-11 22:14:00
firstname	Eva
initial	E
surname	Schmidt
(author)	[LiteratureReference:199781] Congenital glutamine deficiency with glutamine synthetase mutations [LiteratureReference:1258383] The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins [LiteratureReference:9656682] Discovery of cariprazine (RGH-188): a novel antipsychotic acting on dopamine D3/D2 receptors [LiteratureReference:9955754] Identification of novel mutations of the human N-acetylglutamate synthase gene and their functional investigation by expression studies [LiteratureReference:9955766] Mutation analysis in patients with N-acetylglutamate synthase deficiency [LiteratureReference:9958761] Mild citrullinemia in Caucasians is an allelic variant of argininosuccinate synthetase deficiency (citrullinemia type 1)
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No pathways have been reviewed or authored by Schmidt, E (199739)