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• W2035530553 abstract "Human MutationVolume 9, Issue 1 p. 69-71 Mutations in Brief A novel missense point mutation (S134N) of the Cu/Zn superoxide dismutase gene in a patient with familal motor neuron disease M Watanabe, M Watanabe Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, Japan Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorM Aoki, M Aoki Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanSearch for more papers by this authorK Abe, Corresponding Author K Abe Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanDepartment of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanSearch for more papers by this authorM Shoji, M Shoji Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorT Iizuka, T Iizuka Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorY Ikeda, Y Ikeda Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorS Hirai, S Hirai Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorK Kurokawa, K Kurokawa Third Department of Internal Medicine, Yamagata University School of Medicine, Yamagata 990-23, Japan; Fax: 81-22-272-5818Search for more papers by this authorT Kato, T Kato Third Department of Internal Medicine, Yamagata University School of Medicine, Yamagata 990-23, Japan; Fax: 81-22-272-5818Search for more papers by this authorH Sasaki, H Sasaki Third Department of Internal Medicine, Yamagata University School of Medicine, Yamagata 990-23, Japan; Fax: 81-22-272-5818Search for more papers by this authorY Itoyama, Y Itoyama Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanSearch for more papers by this author M Watanabe, M Watanabe Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, Japan Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorM Aoki, M Aoki Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanSearch for more papers by this authorK Abe, Corresponding Author K Abe Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanDepartment of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanSearch for more papers by this authorM Shoji, M Shoji Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorT Iizuka, T Iizuka Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorY Ikeda, Y Ikeda Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorS Hirai, S Hirai Department of Neurology, Gunma University School of Medicine, Gunma 371, JapanSearch for more papers by this authorK Kurokawa, K Kurokawa Third Department of Internal Medicine, Yamagata University School of Medicine, Yamagata 990-23, Japan; Fax: 81-22-272-5818Search for more papers by this authorT Kato, T Kato Third Department of Internal Medicine, Yamagata University School of Medicine, Yamagata 990-23, Japan; Fax: 81-22-272-5818Search for more papers by this authorH Sasaki, H Sasaki Third Department of Internal Medicine, Yamagata University School of Medicine, Yamagata 990-23, Japan; Fax: 81-22-272-5818Search for more papers by this authorY Itoyama, Y Itoyama Department of Neurology, Tohoku University School of Medicine, Sendai 980-77, JapanSearch for more papers by this author First published: 07 January 1999 https://doi.org/10.1002/(SICI)1098-1004(1997)9:1<69::AID-HUMU14>3.0.CO;2-NCitations: 20AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume9, Issue11997Pages 69-71 RelatedInformation" @default.
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• W2035530553 title "A novel missense point mutation (S134N) of the Cu/Zn superoxide dismutase gene in a patient with familal motor neuron disease" @default.
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