Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
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Maung, M. T., Carlson, A., Olea‐Flores, M., Elkhadragy, L., Schachtschneider, K. M., Navarro‐Tito, N., & Padilla‐Benavides, T. (2021) · The FASEB Journal · doi:10.1096/fj.202100273rr · Cited by 157 · see citing works
- Authors
- Rosen, D.
- Corresponding author
- Rosen, Daniel
- Venue
- Nature
- Published
- 1993-07
- Volume
- 364
- Issue
- 6435
- Pages
- 362-362
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W4253140965
- Cited by
- 922
- References
- 0
- Citations by year
- 2026: 18 · 2025: 20 · 2024: 43 · 2023: 39 · 2022: 40 · 2021: 37 · 2020: 42 · 2019: 40 · 2018: 39 · 2017: 38 · 2016: 52 · 2015: 43 · 2014: 44 · 2013: 49 · 2012: 70
- FWCI
- 7.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glutathione Transferases and Polymorphisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Keywords
- Cu/Zn superoxide dismutase, SOD1 gene, familial ALS, genetic mutations, exon 2, protein sequence comparison
- MeSH terms
- Amino Acid Sequence, Animals, Humans, Molecular Sequence Data, Mutation, Superoxide Dismutase, Sequence Homology, Amino Acid
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