Query author contributions in Reactome

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Details on Person Zenker, Martin

Class:Id	Person:6790239
_displayName	Zenker, Martin
_timestamp	2015-08-10 14:38:51
created	[InstanceEdit:6790240] Rothfels, Karen, 2015-08-10
firstname	Martin
initial	M
surname	Zenker
(author)	[LiteratureReference:6790237] Biochemical and functional characterization of germ line KRAS mutations [LiteratureReference:6790346] Germline KRAS mutations cause Noonan syndrome [LiteratureReference:9651003] Diverging gain-of-function mechanisms of two novel KRAS mutations associated with Noonan and cardio-facio-cutaneous syndromes [LiteratureReference:9651267] Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders [LiteratureReference:9660358] Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy [LiteratureReference:9660412] Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair [LiteratureReference:9926078] Human pluripotent stem cell-derived acinar/ductal organoids generate human pancreas upon orthotopic transplantation and allow disease modelling [LiteratureReference:9949735] NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease
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No pathways have been reviewed or authored by Zenker, Martin (6790239)