Query author contributions in Reactome

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Details on Person Heinen, Stefan

Class:Id	Person:4416551
_displayName	Heinen, Stefan
_timestamp	2013-08-26 11:23:45
created	[InstanceEdit:4416538] Shamovsky, V, 2013-08-26
firstname	Stefan
initial	S
surname	Heinen
(author)	[LiteratureReference:4416534] Defective complement control of factor H (Y402H) and FHL-1 in age-related macular degeneration [LiteratureReference:4416621] Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells [LiteratureReference:4416633] Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome [LiteratureReference:4416668] De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome [LiteratureReference:4416670] Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions
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No pathways have been reviewed or authored by Heinen, Stefan (4416551)