Query author contributions in Reactome
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Details on Person van der Graaf, Marinette
| Class:Id | Person:6786688 |
|---|---|
| _displayName | van der Graaf, Marinette |
| _timestamp | 2015-07-09 13:51:15 |
| created | [InstanceEdit:6786674] Jassal, Bijay, 2015-07-09 |
| firstname | Marinette |
| initial | M |
| surname | van der Graaf |
| (author) | [LiteratureReference:6786690] Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia [LiteratureReference:9914306] NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism |
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No pathways have been reviewed or authored by van der Graaf, Marinette (6786688)
