Autosomal dominant amyotrophic lateral sclerosis: a novel mutation in the Cu/Zn superoxide dismutase-1 gene
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/3/12/2261/1831733/3-12-2261.pdf
Cited by 46 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Missense Mutations of Codon 116 in the SOD1 Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype;Frontiers in Genetics;2021-11-17
2. The biophysics of superoxide dismutase-1 and amyotrophic lateral sclerosis;Quarterly Reviews of Biophysics;2019
3. Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene;Neurobiology of Aging;2013-06
4. Copper-Zinc Superoxide Dismutase, Its Copper Chaperone, and Familial Amyotrophic Lateral Sclerosis;Protein Misfolding Diseases;2010-07-02
5. The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families;Journal of Neurology;2010-03-23
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