Article info

Download PDFPDF
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members
  1. Dr G T Plantgordon{at}plant.globalnet.co.uk
View Full Text

Citation

Mead SH, Proukakis C, Wood N, et al
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members

Publication history

  • Received February 2, 2001
  • Revised July 3, 2001
  • Accepted July 6, 2001
  • First published December 1, 2001.
Online issue publication 
April 13, 2016

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.