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Familial Creutzfeldt–Jakob disease with E200K mutation presenting with neurosensorial hypoacusis
  1. Correspondence to:
 R Reñé
 Unitat de Diagnòstic i Tractament de les Demències, Neurology Service, Hospital Universitari de Bellvitge, Feixa Llarga s/n, 08907 L’Hospitalet de Llobregat, Spain;ramonrenye{at}hotmail.com
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Citation

Reñé R, Campdelacreu J, Ferrer I, et al
Familial Creutzfeldt–Jakob disease with E200K mutation presenting with neurosensorial hypoacusis

Publication history

  • First published December 15, 2006.
Online issue publication 
December 15, 2006

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