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Letter
Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation
  1. 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
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Citation

Rohrer JD, Beck J, Warren JD, et al
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 
October 28, 2009

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