Superoxide dismutase (glu100 → gly) in a family with inherited motor neuron disease: detection of mutant superoxide dismutase activity and the presence of heterodimers
- 21 April 1995
- journal article
- case report
- Published by Elsevier in Neuroscience Letters
- Vol. 189 (3) , 143-146
- https://doi.org/10.1016/0304-3940(95)11476-d
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Fast and sensitive silver staining of DNA in polyacrylamide gelsPublished by Elsevier ,2004
- Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in
Cu Zn Journal of the Neurological Sciences, 1994 - Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase MutationScience, 1994
- Rapid Communication: Cu/Zn Superoxide Dismutase Activity in Familial and Sporadic Amyotrophic Lateral SclerosisJournal of Neurochemistry, 1994
- Superoxide Dismutase Activity, Oxidative Damage, and Mitochondrial Energy Metabolism in Familial and Sporadic Amyotrophic Lateral SclerosisJournal of Neurochemistry, 1993
- Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide DismutaseScience, 1993
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993
- Improved double-stranded DNA sequencing using the linear polymerase chain reactionNucleic Acids Research, 1989
- Familial adult motor neuron disease: amyotrophic lateralsclerosisNeurology, 1986
- Superoxide DismutasesAnnual Review of Biochemistry, 1975