Query author contributions in Reactome
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Details on Person Motta, Marialetizia
| Class:Id | Person:9660350 |
|---|---|
| _displayName | Motta, Marialetizia |
| _timestamp | 2019-09-09 19:46:46 |
| created | [InstanceEdit:9660354] Rothfels, Karen, 2019-09-09 |
| firstname | Marialetizia |
| initial | M |
| surname | Motta |
| (author) | [LiteratureReference:9660358] Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy [LiteratureReference:9660380] Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy [LiteratureReference:9660422] SHOC2 subcellular shuttling requires the KEKE motif-rich region and N-terminal leucine-rich repeat domain and impacts on ERK signalling |
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No pathways have been reviewed or authored by Motta, Marialetizia (9660350)
