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Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia
  1. Correspondence to:
 A Brice
 INSERM U679, Groupe Hospitalier Pitié-Salpêtrière, 47 Boulevard de l’Hôpital, 75013 Paris, France; brice{at}ccr.jussieu.fr
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Citation

Depienne C, Fedirko E, Forlani S, et al
Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

Publication history

  • Received September 13, 2006
  • Accepted October 19, 2006
  • Revised October 16, 2006
  • First published November 10, 2006.
Online issue publication 
April 27, 2016

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