Please use this identifier to cite or link to this item:
http://hdl.handle.net/2067/44072| Title: | Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy | Authors: | Motta, M. D'ambrosio, V. Versacci, P. Ventriglia, F. Chillemi, Giovanni Pizzuti, A. Tartaglia, M. De Luca, A. Giancotti, A. Mastromoro, G. Chandramouli, B. Pinna, V. Pantaleoni, F. Di Giosaffatte, N. Petrini, S. Mazza, T. |
Journal: | HUMAN MUTATION | Issue Date: | 2019 | URI: | http://hdl.handle.net/2067/44072 | DOI: | 10.1002/humu.23767 |
| Appears in Collections: | A1. Articolo in rivista |
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