A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy

Por Muglia, M, Vazza, G, Patitucci, A, Milani, M, Pareyson, D, Taroni, F, Quattrone, A, Mostacciuolo, M L
Publicado em 2007

Childhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies

Por Ruggieri, M., Praticò, A.D., Serra, A., Maiolino, L., Cocuzza, S., Di Mauro, P., Licciardello, L., Milone, P., Privitera, G., Belfiore, G., Di Pietro, M., Di Raimondo, F., Romano, A., Chiarenza, A., Muglia, M., Polizzi, A., Evans, D.G.
Publicado no Acta Otorhinolaryngol Ital (2016)