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Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutation
  1. Correspondence to:
 Dr David O Robinson
 Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire SP2 8BJ, UK; david.robinson{at}salisbury.nhs.uk
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Citation

Robinson DO, Wills AJ, Hammans SR, et al
Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutation

Publication history

  • Received August 2, 2005
  • Accepted September 19, 2005
  • Revised September 15, 2005
  • First published April 28, 2006.
Online issue publication 
April 28, 2006

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