Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features.
Open Access
- 1 December 1996
- journal article
- review article
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 61 (6), 565-572
- https://doi.org/10.1136/jnnp.61.6.565
Abstract
No abstract availableThis publication has 76 references indexed in Scilit:
- Apoptosis and increased generation of reactive oxygen species in Down's syndrome neurons in vitroNature, 1995
- Toxic mutants in Charcot's sclerosisNature, 1995
- Superoxide dismutase (glu100 → gly) in a family with inherited motor neuron disease: detection of mutant superoxide dismutase activity and the presence of heterodimersNeuroscience Letters, 1995
- A New Variant Cu/Zn Superoxide Dismutase (Val7→Glu) Deduced from Lymphocyte mRNA Sequences from Japanese Patients with Familial Amyotrophic Lateral SclerosisBiochemical and Biophysical Research Communications, 1994
- Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosisNeuron, 1994
- A Novel Mutation in Cu/Zn Superoxide Dismutase Gene in Japanese Familial Amyotrophic Lateral SclerosisBiochemical and Biophysical Research Communications, 1994
- The Cu/Zn superoxide dismutase gene in ALS and Parkinsonism-dementia of GuamNeuroReport, 1994
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993
- Evolutionary Aspects of Superoxide Dismutase: The Copper/Zinc EnzymeFree Radical Research Communications, 1991
- Down's syndrome: Abnormal neuromuscular junction in tongue of transgenic mice with elevated levels of human Cu/Zn-superoxide dismutaseCell, 1988