Valérie Briolotti

Association between centromeric deletions of the SMN gene and sporadic adult‐onset lower motor neuron disease

A. Malafosse, V. Meininger, F. Salachas, 1998, Annals of neurology.

Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family

G. Rouleau, W. Camu, P. Clavelou, 2001, Annals of neurology.