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Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia
  1. Correspondence to:
 Dr A Bouhouche
 Service de Neurologie et de Neurogénétique, Hôpital des Spécialités, BP 6402, Al Irfane Rabat, Morocco; abouhouche{at}hotmail.com
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Citation

Bouhouche A, Benomar A, Bouslam N, et al
Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia

Publication history

  • Accepted December 21, 2005
  • Revised December 19, 2005
  • First published January 6, 2006.
Online issue publication 
April 28, 2006

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