Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations

P. Corcia, P. Valdmanis, S. Millecamps, C. Lionnet, H. Blasco, K. Mouzat, H. Daoud, V. Belzil, R. Morales, N. Pageot, V. Danel-Brunaud, N. Vandenberghe, P. F. Pradat, P. Couratier, F. Salachas, S. Lumbroso, G. A. Rouleau, V. Meininger, W. Camu