Query author contributions in Reactome

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Details on Person D'Eustachio, P, 2013-11-18

Class:Id	InstanceEdit:5146702
_displayName	D'Eustachio, P, 2013-11-18
_timestamp	2013-11-18 14:56:19
author	[Person:140934] D'Eustachio, Peter
dateTime	2013-11-18 19:56:12
(modified)	[FailedReaction:3229118] Defective SLC37A4 does not exchange G6P and Pi across the ER membrane [Homo sapiens] [Pathway:3229121] Glycogen storage diseases [Homo sapiens] [Pathway:3229133] Glycogen storage disease type Ib (SLC37A4) [Homo sapiens] [Pathway:3274531] Glycogen storage disease type Ia (G6PC) [Homo sapiens] [FailedReaction:3274540] Defective G6PC does not hydrolyze glucose 6-phosphate [Homo sapiens] [Pathway:3282872] Severe congenital neutropenia type 4 (G6PC3) [Homo sapiens] [FailedReaction:3282876] Defective G6PC3 does not hydrolyze glucose 6-phosphate [Homo sapiens] [Pathway:3785653] Myoclonic epilepsy of Lafora [Homo sapiens] [FailedReaction:3791349] Defective EPM2A does not dephosphorylate phosphoglycogen (type 2A disease) [Homo sapiens] [FailedReaction:3797226] Defective NHLRC1 does not ubiquitinate EPM2A (laforin) and PPP1R3C (PTG) (type 2B disease) [Homo sapiens] List all 18 refering instances
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No pathways have been reviewed or authored by D'Eustachio, P, 2013-11-18 (5146702)