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Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia
- Correspondence to: A Brice INSERM U679, Groupe Hospitalier Pitié-Salpêtrière, 47 Boulevard de l’Hôpital, 75013 Paris, France; brice{at}ccr.jussieu.fr
Citation
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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Copyright 2007 Journal of Medical Genetics