Query author contributions in Reactome

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Details on Person Skerka, Christine

Class:Id	Person:4416559
_displayName	Skerka, Christine
_timestamp	2013-08-26 11:23:51
created	[InstanceEdit:4416538] Shamovsky, V, 2013-08-26
firstname	Christine
initial	C
surname	Skerka
(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: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 [LiteratureReference:5148672] The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome [LiteratureReference:8851448] Human factor H-related protein 2 (CFHR2) regulates complement activation [LiteratureReference:9855693] Kallikrein Cleaves C3 and Activates Complement
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No pathways have been reviewed or authored by Skerka, Christine (4416559)