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Excitability properties of mouse motor axons in the mutant SOD1G93A model of amyotrophic lateral sclerosis

✍ Scribed by Delphine Boërio; Bernadett Kalmar; Linda Greensmith; Hugh Bostock

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
590 KB
Volume
41
Category
Article
ISSN
0148-639X

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## Abstract ## Background and Objective Familial amyotrophic lateral sclerosis (FALS) is a neurodegenerative disease characterized by progressive loss of motor neurons and death. Mitochondrial dysfunction and oxidative stress play an important role in motor neuron loss in ALS. Light therapy (LT) h