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.
If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.
Details on Person Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia
| Class:Id | LiteratureReference:449316 |
|---|---|
| _displayName | Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia |
| _timestamp | 2009-12-02 11:34:46 |
| author | [Person:201393] Sun, L [Person:449232] Eklund, EA [Person:449306] Chung, WK [Person:169524] Wang, C [Person:449257] Cohen, J [Person:449265] Freeze, HH |
| created | [InstanceEdit:449318] Jassal, B, 2009-12-02 |
| journal | J Clin Endocrinol Metab |
| pages | 4371-5 |
| pubMedIdentifier | 15840742 |
| title | Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia |
| volume | 90 |
| year | 2005 |
| (literatureReference) | [Reaction:446188] ALG3 transfers Man to N-glycan precursor (GlcNAc)2 (Man)5 (PP-Dol)1 [Homo sapiens] [FailedReaction:4720473] Defective ALG3 does not add mannose to the N-glycan precursor [Homo sapiens] [Pathway:4720475] Defective ALG3 causes CDG-1d [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia (449316)
