Query author contributions in Reactome

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Details on Person Rutsch, F

Class:Id	Person:199755
_displayName	Rutsch, F
_timestamp	2007-07-11 22:14:22
created	[InstanceEdit:199761] D'Eustachio, P, 2007-07-11 22:14:00
firstname	Frank
initial	F
surname	Rutsch
(author)	[LiteratureReference:199781] Congenital glutamine deficiency with glutamine synthetase mutations [LiteratureReference:200178] beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities [LiteratureReference:3000283] Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism [LiteratureReference:3159284] Insights into lysosomal cobalamin trafficking: lessons learned from cblF disease [LiteratureReference:3928676] Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism
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No pathways have been reviewed or authored by Rutsch, F (199755)