Amyotrophic Lateral Sclerosis (ALS) is generally a late onset neurodegenerative disease. Mutations in the Cu/Zn superoxide dismutase 1 (SOD1) gene accounts for approximately 20% of familial ALS and 2%
Additional file 6. HCA and HSP genes. The file contains HCA and HSP genes found differentially expressed in each of the three cell lines analyzed (LCLs, FCLs, iPSC-derived neurons).