Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference13 articles.
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2. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis;Rosen;Nature,1993
3. New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1(SOD-1) gene mutations: inclusions containing SOD-1 in neurons and astrocytes;Kato;ALS,2000
4. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation;Jackson;Ann. Neurol.,1997
5. An improved protocol for the analysis of SOD-1 gene mutations, and a new mutation in exon 4;Yulug;Hum. Mol. Genet.,1995
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1. Copper-Zinc Superoxide Dismutase, Its Copper Chaperone, and Familial Amyotrophic Lateral Sclerosis;Protein Misfolding Diseases;2010-07-02
2. Protein Aggregation and Protein Instability Govern Familial Amyotrophic Lateral Sclerosis Patient Survival;PLoS Biology;2008-07-29
3. HIF1 and oxygen sensing in the brain;Nature Reviews Neuroscience;2004-06
4. Neurophysiology of hereditary amyotrophic lateral sclerosis;Handbook of Clinical Neurophysiology;2004
5. Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes;AMYOTROPH LATERAL SC;2003
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