Clinical testing and spinal cord removal in a mouse model for amyotrophic lateral sclerosis (ALS).

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder resulting in progressive degeneration of motoneurons. Peak of onset is around 60 years for the sporadic disease and around 50 years for the familial disease. Due to its progressive course, 50% of the patients die within 30 months of symptom onset. In order to evaluate novel treatment… (More)
DOI: 10.3791/3936

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