Spinocerebellar ataxia type 2: A clinical, molecular, neurochemical and electrophysiological study of the mutation in 106 Cuban families - Velazquez-Perez, L; Sanchez-Cruz, G; Galicia-Polo, L; Auburger, G; Garcia-Rodriguez, J; Rodriguez-Labrada, R; Almaguer-Mederos, L; Coello-Almarales, D; Laffita-Mesa, J; Aguilera-Rodriguez, R; Gonzalez, C; Cannales-Ochoa, N (MOVEMENT DISORDERS, 2009)