Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy: Human molecular genetics

M. Motta, L. Sagi-Dain, O.H.F. Krumbach, A. Hahn, A. Peleg, A. German, C. Lissewski, S. Coppola, F. Pantaleoni, L. Kocherscheid, F. Altmüller, D. Schanze, T. Logeswaran, S. Chahrokh-Zadeh, A. Munzig, S. Nakhaei-Rad, H. Cavé, M.R. Ahmadian, M. Tartaglia, M. Zenker

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Medicine & Life Sciences