R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease. by Beffagna, G, Cecchetto, A, Dal Bianco, L, Lorenzon, A, Angelini, A, Padalino, M, Vida, V, Bhattacharya, S, Stellin, G, Rampazzo, A, Daliento, L

Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro by Beffagna, G, De Bortoli, M, Nava, A, Salamon, M, Lorenzon, A, Zaccolo, M, Mancuso, L, Sigalotti, L, Bauce, B, Occhi, G, Basso, C, Lanfranchi, G, Towbin, J, Thiene, G, Danieli, G, Rampazzo, A