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Letter
Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation
- Correspondence to Dr S Mead, MRC Prion Unit, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK; s.mead{at}prion.ucl.ac.uk
Citation
Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation
Publication history
- Received December 19, 2008
- Revised February 10, 2009
- Accepted February 17, 2009
- First published October 28, 2009.
Online issue publication
April 13, 2016
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