A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis

Published:1995 Issue:3 Volume:4 Page:491-492
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Ikeda M.,Abe K.,Ogasawara M.,Kameya T.,Watanabe M.,Shoji M.,Hirai S.,Itoyama Y.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/4/3/491/1586148/4-3-491.pdf

Cited by 29 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. The biophysics of superoxide dismutase-1 and amyotrophic lateral sclerosis;Quarterly Reviews of Biophysics;2019

2. Pathophysiology of Neurodegeneration in Familial Amyotrophic Lateral Sclerosis;Current Molecular Medicine;2009-04-01

3. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation;Acta Neuropathologica;2004-07-03

4. 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

5. Chapter 8 Genetic Aspects of Amyotrophic Lateral Sclerosis/Motor Neuron Disease;Motor Neuron Disorders;2003

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