Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family
Trinchillo, Assunta, Valente, Valeria, Esposito, Marcello, Migliaccio, Miriana, Iovino, Aniello, Picciocchi, Michele, Cuomo, Nunzia, Caccavale, Carmela, Nocerino, Cristofaro, De Rosa, Laura, Salvatore, Elena, Pierantoni, Giovanna Maria, Menchise, Valeria, Paladino, Simona, Criscuolo, Chiara
Published in Neurological sciences (01.09.2024)
Published in Neurological sciences (01.09.2024)
Get full text
Journal Article