Age-dependent degeneration of an identified adult leg motor neuron in a Drosophila SOD1 model of ALS
Mutations in superoxide dismutase 1 (SOD1) cause familial amyotrophic lateral sclerosis (ALS) in humans. ALS is a neurodegenerative disease characterized by progressive motor neuron loss leading to paralysis and inevitable death in affected individuals. Using a gene replacement strategy to introduce...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
The Company of Biologists
2020-10-01
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Series: | Biology Open |
Subjects: | |
Online Access: | http://bio.biologists.org/content/9/10/bio049692 |