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Short report
The human G93A SOD1 phenotype closely resembles sporadic amyotrophic lateral sclerosis
- Correspondence to Dr M Synofzik, Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, Hoppe-Seyler-Str 3, University of Tübingen, Tübingen 72076, Germany; matthis.synofzik{at}uni-tuebingen.de
Citation
The human G93A SOD1 phenotype closely resembles sporadic amyotrophic lateral sclerosis
Publication history
- Received April 27, 2009
- Revised June 3, 2009
- Accepted June 16, 2009
- First published February 22, 2010.
Online issue publication
June 25, 2010
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- Previous version (22 February 2010).
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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.