Query author contributions in Reactome

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Details on Person Gerardy-Schahn, Rita

Class:Id	Person:742367
_displayName	Gerardy-Schahn, Rita
_timestamp	2013-04-10 16:38:17
created	[InstanceEdit:742359] Jassal, Bijay, 2010-05-17
firstname	Rita
initial	R
modified	[InstanceEdit:3262502] D'Eustachio, P, 2013-04-10
surname	Gerardy-Schahn
(author)	[LiteratureReference:742376] The human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamine [LiteratureReference:3262510] A syndrome with congenital neutropenia and mutations in G6PC3 [LiteratureReference:3702132] ST3GAL3 mutations impair the development of higher cognitive functions [LiteratureReference:3702145] West syndrome caused by ST3Gal-III deficiency [LiteratureReference:5653606] Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis [LiteratureReference:9927102] Identification of glycosyltransferase 8 family members as xylosyltransferases acting on O-glucosylated notch epidermal growth factor repeats
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No pathways have been reviewed or authored by Gerardy-Schahn, Rita (742367)