Query author contributions in Reactome

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Details on Person Matthijs, Gert

Class:Id	Person:3781855
_displayName	Matthijs, Gert
_timestamp	2013-06-28 13:04:36
created	[InstanceEdit:3781876] Jassal, B, 2013-06-28
firstname	Gert
initial	G
surname	Matthijs
(author)	[LiteratureReference:3781875] Congenital disorders of glycosylation: a review [LiteratureReference:4549383] CDG nomenclature: time for a change! [LiteratureReference:4719379] DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy [LiteratureReference:4836527] Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation [LiteratureReference:5609943] Multiple phenotypes in phosphoglucomutase 1 deficiency [LiteratureReference:5615510] Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip [LiteratureReference:5690644] Congenital disorders of glycosylation: a rapidly expanding disease family [LiteratureReference:8955667] Mammalian phosphomannomutase PMM1 is the brain IMP-sensitive glucose-1,6-bisphosphatase [LiteratureReference:9859455] Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects [LiteratureReference:9937278] A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesis
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No pathways have been reviewed or authored by Matthijs, Gert (3781855)