A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis

Published:1994 Issue:6 Volume:3 Page:981-987
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Rosen Daniel R.,Bowling Allen C.,Patterson David,Usdin Ted B.,Sapp Peter,Mezey Eva,McKenna-Yasek Diane,O'Regan Jerimiah,Rahmani Zohra,Ferrante Robert J.,Brownstein Michael J.,Kowall Neil W.,Beal M.Flint,Horvitz H.Robert,Brown Robert H.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/3/6/981/1608428/3-6-981.pdf

Cited by 146 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. Clinical characterization of common pathogenic variants of SOD1-ALS in Germany;Journal of Neurology;2024-08-14

2. Effects of Pathogenic Mutants of the Neuroprotective RNase 5-Angiogenin in Amyotrophic Lateral Sclerosis (ALS);Genes;2024-06-04

3. Pan-neuronal expression of human mutant SOD1 in Drosophila impairs survival and motor performance, induces early neuroinflammation and chromosome aberrations;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-06

4. Variability in SOD1-associated amyotrophic lateral sclerosis: geographic patterns, clinical heterogeneity, molecular alterations, and therapeutic implications;Translational Neurodegeneration;2024-05-29

5. Ebselen analogues delay disease onset and its course in fALS by on-target SOD-1 engagement;Scientific Reports;2024-05-27