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Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
- Correspondence to Dr L Schöls, Department of Neurology, University of Tübingen, Hoppe-Seyler-Str 3, D 72076 Tübingen, Germany; ludger.schoels{at}uni-tuebingen.de
Citation
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
Publication history
- Received November 7, 2008
- Revised January 30, 2009
- Accepted February 12, 2009
- First published November 16, 2009.
Online issue publication
April 13, 2016
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