Michael Horwich, W. King Engel, P. B. Chauvin
Abstract
Sera from patients with amyotrophic lateral sclerosis (ALS) were applied to mouse anterior horn cells in tissue culture. No unique toxic effect was observed when compared with sera from normal and non-ALS neuromuscular disease subjects.
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Sera from patients with amyotrophic lateral sclerosis (ALS) were applied to mouse anterior horn cells in tissue culture. No unique toxic effect was observed when compared with sera from normal and non-ALS neuromuscular disease subjects.
Key concepts: Amyotrophic lateral sclerosis, Anterior Horn Cell, Motor neuron, Medicine, Motor neurone disease, Neuroscience, Pathology, Biology