Query author contributions in Reactome

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Details on Person Riemersma, Moniek

Class:Id	Person:4719392
_displayName	Riemersma, Moniek
_timestamp	2013-10-18 14:44:03
created	[InstanceEdit:4719380] Jassal, B, 2013-10-18
firstname	Moniek
initial	M
surname	Riemersma
(author)	[LiteratureReference:4719379] DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy [LiteratureReference:4755618] Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation [LiteratureReference:9940672] Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation [LiteratureReference:9940798] Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome
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No pathways have been reviewed or authored by Riemersma, Moniek (4719392)