Reactome: A Curated Pathway Database
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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person Van Schaftingen, E

Class:IdPerson:3781853
_displayNameVan Schaftingen, E
_timestamp2013-06-28 13:04:35
created[InstanceEdit:3781876] Jassal, B, 2013-06-28
firstnameE
initialE
surnameVan Schaftingen
(author)[LiteratureReference:3781828] Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation
[LiteratureReference:3781859] High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency)
[LiteratureReference:3781897] Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A
[LiteratureReference:6799503] D-glycerate kinase deficiency as a cause of D-glyceric aciduria
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No pathways have been reviewed or authored by Van Schaftingen, E (3781853)