1. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase;Andersen, P.M.; Nilsson, P.; Ala-Hurula, V.; Keranen, M.-L.; Tarvainen, I.; Haltia, T.;Nature Genetics; Professor D Vassipoulos,1995
2. A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis;Ikeda, M.; Abe, K.; Aoki, M.; Ogasawara, M.; Kameya, T.; Watanabe, M.;Hum Mol Genet,1995
3. Fisher EMC. An improved protocol for the analysis of SODI gene mutations, and a new mutation in exon 4. Hum Mol Genet;Yulug, I.G.; Katsanis, N.; de Belleroche, J.; Collinge, J.;Arch Physiol; Deux cas d'atrophie musculaire progressive avec lesions de la substance grise et des faisceaux antero-lateraux de la moelle epiniere,1995
4. Two novel SODI mutations in patients with familial amyotrophic lateral sclerosis;Deng, H.-X.; Tainer, J.A.; Mitsumoto, H.; Ohnishi, A.; He, X.; Hung, W.-Y.;Hum Mol Neurol Path; Genet,1995
5. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lat- 28 Enayat;Rosen, D.R.; Siddique, T.; Patterson, D.; Figlewicz, D.A.; Sapp, P.; Hentati, A.;Nature; Two novel mutations in the gene for copper zinc superoxide dismutase in UK families with eral sclerosis,1993