Misfolded SOD1 and ALS: Zeroing in on mitochondria
Author:
Publisher
Informa UK Limited
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/17482968.2012.648645
Reference52 articles.
1. Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1
2. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
3. Non–cell autonomous toxicity in neurodegenerative disorders: ALS and beyond
4. Aggregation of Mutant Cu/Zn Superoxide Dismutase Proteins in a Culture Model of ALS
5. Variation in aggregation propensities among ALS-associated variants of SOD1: Correlation to human disease
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