Query author contributions in Reactome

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Details on Person Schuelke, Markus

Class:Id	Person:164795
_displayName	Schuelke, Markus
_timestamp	2015-06-17 20:38:08
created	[InstanceEdit:164783] Jassal, Bijay, 2005-06-21
firstname	Markus
initial	M
modified	[InstanceEdit:508032] D'Eustachio, P, 2010-02-10 [InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17
surname	Schuelke
(author)	[LiteratureReference:164765] cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: [LiteratureReference:508064] Mutations in PYCR1 cause cutis laxa with progeroid features [LiteratureReference:6802076] Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1 [LiteratureReference:9916618] Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
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No pathways have been reviewed or authored by Schuelke, Markus (164795)