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Short report
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype

Authors

  1. Prof. José Berciano, Service of Neurology, “Marqués de Valdecilla” University Hospital, 39008 Santander, Spain; jaberciano{at}humv.es
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Citation

Berciano J, Gallardo E, Domínguez-Perles R, et al
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype
Journal of Neurology, Neurosurgery & Psychiatry 2008;79:205-208.

Publication history

  • Received May 21, 2007
  • Revised July 12, 2007
  • Accepted July 16, 2007
  • First published August 13, 2007.
Online issue publication 
April 13, 2016

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2008 BMJ Publishing Group