Query author contributions in Reactome

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Details on Person Orlic-Milacic, Marija, 2024-08-15

Class:Id	InstanceEdit:9918437
_displayName	Orlic-Milacic, Marija, 2024-08-15
_timestamp	2024-08-15 16:06:56
author	[Person:1169272] Orlic-Milacic, Marija
dateTime	2024-08-15 16:06:48
(created)	[DefinedSet:9918435] OPN1MW LOF variants [photoreceptor disc membrane] [Homo sapiens] [Pathway:9918436] Defective visual phototransduction due to OPN1MW loss of function [Homo sapiens] [Pathway:9918438] Defective visual phototransduction due to RDH5 loss of function [Homo sapiens] [Disease:9918439] color blindness [Pathway:9918440] Defective visual phototransduction due to RDH12 loss of function [Homo sapiens] [Summation:9918441] 11-cis-retinol dehydrogenase (RDH5) can reversibly catalyse ... [Pathway:9918442] Defective visual phototransduction due to LRAT loss of function [Homo sapiens] [Pathway:9918443] Defective visual phototransduction due to OPN1SW loss of function [Homo sapiens] [LiteratureReference:9918444] Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms [InstanceEdit:9918445] Matthews, Lisa, 2024-08-15 List all 32 refering instances
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No pathways have been reviewed or authored by Orlic-Milacic, Marija, 2024-08-15 (9918437)