Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy.
- Resource Type
- Article
- Authors
- Motta, Marialetizia; Sagi-Dain, Lena; Krumbach, Oliver H F; Hahn, Andreas; Peleg, Amir; German, Alina; Lissewski, Christina; Coppola, Simona; Pantaleoni, Francesca; Kocherscheid, Luisa; Altmüller, Franziska; Schanze, Denny; Logeswaran, Thushiha; Chahrokh-Zadeh, Soheyla; Munzig, Anna; Nakhaei-Rad, Saeideh; Cavé, Hélène; Ahmadian, Mohammad R; Tartaglia, Marco; Zenker, Martin
- Source
- Human Molecular Genetics; Jun2020, Vol. 29 Issue 11, p1772-1783, 12p
- Subject
- Language
- ISSN
- 09646906