Accumulation of misfolded SOD1 outlines distinct patterns of motor neuron pathology and death during disease progression in a SOD1 G93A mouse model of amyotrophic lateral sclerosis
Author:
Affiliation:
1. Patologia Neuromuscular Experimental, Departament de Medicina Experimental, Facultat de Medicina Universitat de Lleida and Institut de Recerca Biomèdica de Lleida (IRBLleida) Lleida Catalonia Spain
Funder
Ministerio de Ciencia e Innovación
Ministerio de Educación, Cultura y Deporte
Publisher
Wiley
Subject
Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.13078
Reference144 articles.
1. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
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3. Lessons from models of SOD1-linked familial ALS
4. Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis
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