Mutations in all five exons ofSOD-1 may cause ALS
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference19 articles.
1. Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction
2. Familial Amyotrophic Lateral Sclerosis, 1850-1989: A Statistical Analysis of the World Literature
3. Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide Dismutase
4. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
5. Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase.
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