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Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum

Authors

  1. Dr M T Bassi, Laboratory of Molecular Biology, E. Medea Scientific Institute, Via D. L. Monza 20, 23842 Bosisio Parini, Lecco, Italy; mariateresa.bassi{at}bp.lnf.it
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Citation

Crimella C, Arnoldi A, Crippa F, et al
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum
Journal of Medical Genetics 2009;46:345-351.

Publication history

  • Received September 17, 2008
  • Revised November 28, 2008
  • Accepted December 24, 2008
  • First published February 5, 2009.
Online issue publication 
April 27, 2016

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2009 BMJ Publishing Group