Browsing by Author Petrini, S.


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Issue DateTitleAuthor(s)
2019Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathyMotta, 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.