Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.

Author:

Jones C T,Swingler R J,Simpson S A,Brock D J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic locus heterogeneity;Siddique, T.; Figlewicz, D.A.; Pericak-Vance, M.A.;N Engl_r Med,1991

2. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis;Rosen, D.R.; Siddique, T.; Patterson, D.;Nature,1993

3. Oxygen radicals and the nervous system;Halliwell, B.; Gutteridge, J.M.C.;Trends Neurosci,1985

4. Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase. EMBOJ7;Levanon, D.; Lieman-Hurwitz, J.; Dafni, N.,1985

5. Amyotrophic lateral sclerosis and structural defects in Cu, Zn superoxide dismutase;Deng, H.X.; Hentati, A.; Tainer, J.A.;Science,1993

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