Author:
Nakanishi Toyofumi,Kishikawa Masahiko,Miyazaki Ayako,Shimizu Akira,Ogawa Yasuko,Sakoda Saburo,Ohi Takekazu,Shoji Hiroshi
Reference14 articles.
1. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase;Andersen;Nat Genet,1995
2. Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity;Borchelt;Proc Natl Acad Sci USA,1994
3. ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions;Bruijn;Neuron,1997
4. Advances in ALS;Gutmann;Neurology,1996
5. Kadekawa J, Fujimura H, Ogawa Y, Hattori N, Kaido M, Nishimura T, Yoshikawa H, Shirahata N, Sakoda S, Yanagihara T. A clinicopathological study of a patient with familial amyotrophic lateral sclerosis associated with a two base pair deletion in the SOD1 gene. Acta Neuropathol (in press).
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