A novel two-base mutation in the Cu Zn
- 23 February 1996
- journal article
- Published by Elsevier in Neuroscience Letters
- Vol. 205 (2) , 79-82
- https://doi.org/10.1016/0304-3940(96)12378-8
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
This publication has 11 references indexed in Scilit:
- Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel cu/zn superoxide dismutase mutationAnnals of Neurology, 1995
- Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutaseNature Genetics, 1995
- Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.Journal of Medical Genetics, 1995
- Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in
Cu Zn Journal of the Neurological Sciences, 1994 - 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
- A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosisHuman Molecular Genetics, 1994
- A Novel Mutation in Cu/Zn Superoxide Dismutase Gene in Japanese Familial Amyotrophic Lateral SclerosisBiochemical and Biophysical Research Communications, 1994
- 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
- Reevaluation of assay methods and establishment of kit for superoxide dismutase activityAnalytical Biochemistry, 1984