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Details on Person Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy
| Class:Id | LiteratureReference:9660358 |
| _displayName | Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy |
| _timestamp | 2019-09-09 19:46:48 |
| author | [Person:9660350] Motta, Marialetizia [Person:9660345] Sagi-Dain, Lena [Person:9660359] Krumbach, Oliver H F [Person:9660353] Hahn, Andreas [Person:9660352] Peleg, Amir [Person:9660355] German, Alina [Person:9660361] Lissewski, Christina [Person:9660357] Coppola, Simona [Person:9651014] Pantaleoni, Francesca [Person:9660349] Kocherscheid, Luisa [Person:9660360] Altmüller, Franziska [Person:9660344] Schanze, Denny [Person:9660351] Logeswaran, Thushiha [Person:9660356] Chahrokh-Zadeh, Soheyla [Person:9660346] Munzig, Anna [Person:9660347] Nakhaei-Rad, Saeideh [Person:5683213] Cavé, Hélène [Person:9660348] Ahmadian, Mohammad R [Person:2060728] Tartaglia, M [Person:6790239] Zenker, Martin |
| created | [InstanceEdit:9660354] Rothfels, Karen, 2019-09-09 |
| journal | Hum. Mol. Genet. |
| pubMedIdentifier | 31108500 |
| title | Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy |
| year | 2019 |
| (literatureReference) | [EntityWithAccessionedSequence:9660508] S-GGC MRAS G23R [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9660514] S-GGC MRAS T68I [plasma membrane] [Homo sapiens] [Pathway:9660537] Signaling by MRAS-complex mutants [Homo sapiens] [Reaction:9660538] Mutant MRAS:SHOC2:PPP1CC complexes dephosphorylate inactive RAFs [Homo sapiens] |
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No pathways have been reviewed or authored by Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy (9660358)