Query author contributions in Reactome

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Details on Person Jassal, B, 2012-04-27

Class:Id	InstanceEdit:2210366
_displayName	Jassal, B, 2012-04-27
_timestamp	2012-04-27 16:03:05
author	[Person:73447] Jassal, Bijay
dateTime	2012-04-27 20:02:37
(created)	[EntityWithAccessionedSequence:2210360] IDS (34-455) R443* [lysosomal lumen] [Homo sapiens] [EntityWithAccessionedSequence:2210361] IDS (456-550) R468G [lysosomal lumen] [Homo sapiens] [DefinedSet:2210362] IDS mutants [lysosomal lumen] [Homo sapiens] [ReplacedResidue:2210363] L-arginine 468 replaced with L-leucine [EntityWithAccessionedSequence:2210364] IDS (456-550) R468L [lysosomal lumen] [Homo sapiens] [ReplacedResidue:2210365] L-arginine 468 replaced with glycine [NonsenseMutation:2210367] Nonsense mutation at L-arginine 443 [EntityWithAccessionedSequence:2210368] IDS (456-550) R468W [lysosomal lumen] [Homo sapiens] [ReplacedResidue:2210369] L-arginine 468 replaced with L-tryptophan [Disease:2210370] mucopolysaccharidosis II
(modified)	[PathwayDiagram:1836730] Diagram of Glycosaminoglycan metabolism [Summation:2206289] Mucopolysaccharidosis II (MPS II, Hunter syndrome, MIM:30990... [Summation:2206295] Absence of alpha-L-iduronidase (IDUA, MIM:252800), the enzym... [Pathway:2206296] MPS II - Hunter syndrome (HS-GAG degradation) [Homo sapiens] [FailedReaction:2206299] Defective IDUA does not hydrolyse Heparan sulfate chain(6) [Homo sapiens] [Summation:2206301] Mucopolysaccharidosis type I (MPS I, Hurler syndrome, Hurler... [DefinedSet:2207701] IDUA mutants [lysosomal lumen] [Homo sapiens] [FailedReaction:9036037] Defective IDUA does not hydrolyse Heparan sulfate chain(1) [Homo sapiens] [FailedReaction:9036041] Defective IDUA does not hydrolyse the unsulfated alpha-L-iduronosidic link in DS [Homo sapiens]
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No pathways have been reviewed or authored by Jassal, B, 2012-04-27 (2210366)