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Autor:
Marie-Soleil Lamarre, François-Dominique Scott, Peter Gould, François Berthod, Nicolas Dupré, Lydia Touzel-Deschênes, François Gros-Louis, Jean-Pierre Bouchard, Hélène T. Khuong, Guy A. Rouleau, Rémy Lamontagne, Patrick A. Dion, Bastien Paré
Publikováno v:
Acta Neuropathologica Communications
Amyotrophic lateral sclerosis (ALS) is an adult-onset disease characterized by the selective degeneration of motor neurons in the brain and spinal cord progressively leading to paralysis and death. Current diagnosis of ALS is based on clinical assess