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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
- Correspondence to: Dr A Bouhouche Service de Neurologie et de Neurogénétique, Hôpital des Spécialités, BP 6402, Al Irfane Rabat, Morocco; abouhouche{at}hotmail.com
Citation
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 27, 2016
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Copyright 2006 Journal of Medical Genetics