Browsing by Author Motta, M.

Showing results 1 to 2 of 2
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.
2016SHOC2 subcellular shuttling requires the KEKE motif-rich region and N-terminal leucine-rich repeat domain and impacts on ERK signalingMotta, M.; Tartaglia, M.; Chillemi, Giovanni ; Fodale, V.; Cecchetti, S.; Coppola, S.; Stipo, S.; Cordeddu, V.; Macioce, P.; Gelb Bd