Query author contributions in Reactome
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Details on Person Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS
| Class:Id | LiteratureReference:6787739 |
|---|---|
| _displayName | Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS |
| _timestamp | 2015-07-16 14:22:07 |
| author | [Person:1606515] Vandenberghe, P [Person:6787726] Beel, Karolien |
| created | [InstanceEdit:6787740] Jupe, Steve, 2015-07-16 |
| journal | Pediatr Rep |
| pages | e9 |
| pubMedIdentifier | 22053285 |
| title | Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS |
| volume | 3 |
| year | 2011 |
| (literatureReference) | [Summation:6787736] The granulocyte colony-stimulating factor receptor (CSF3R, G... [Pathway:9674555] Signaling by CSF3 (G-CSF) [Homo sapiens] |
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No pathways have been reviewed or authored by Severe congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS (6787739)
