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Age-dependent degeneration of an identified adult leg motor neuron in a Drosophila SOD1 model of ALS
Autor:
Anthony Agudelo, Victoria St. Amand, Lindsey Grissom, Danielle Lafond, Toni Achilli, Asli Sahin, Robert Reenan, Geoff Stilwell
Publikováno v:
Biology Open, Vol 9, Iss 10 (2020)
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 individua
Externí odkaz:
https://doaj.org/article/79baea328697445ea22521ddb17071fc
