Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

par Conidi, Maria E., Bernardi, Livia, Puccio, Gianfranco, Smirne, Nicoletta, Muraca, Maria G., Curcio, Sabrina A.M., Colao, Rosanna, Piscopo, Paola, Gallo, Maura, Anfossi, Maria, Frangipane, Francesca, Clodomiro, Alessandra, Mirabelli, Maria, Vasso, Franca, Cupidi, Chiara, Torchia, Giusi, Di Lorenzo, Raffaele, Mandich, Paola, Confaloni, Annamaria, Maletta, Raffaele G., Bruni, Amalia C.
Publié dans Neurology (2015)

Mutation analysis of CHCHD10 in different neurodegenerative diseases

par Zhang, Ming, Xi, Zhengrui, Zinman, Lorne, Bruni, Amalia C., Maletta, Raffaele G., Curcio, Sabrina A. M., Rainero, Innocenzo, Rubino, Elisa, Pinessi, Lorenzo, Nacmias, Benedetta, Sorbi, Sandro, Galimberti, Daniela, Lang, Anthony E., Fox, Susan, Surace, Ezequiel I., Ghani, Mahdi, Guo, Jing, Sato, Christine, Moreno, Danielle, Liang, Yan, Keith, Julia, Traynor, Bryan J., St George-Hyslop, Peter, Rogaeva, Ekaterina
Publié dans Brain (2015)