Published February 1, 2017 | Version Accepted Version
Journal article Open

KCNA2 mutations are rare in hereditary spastic paraplegia

Authors/Creators

  • 1. Montreal Neurological Institute and Hospital; McGill University; Montreal Quebec
  • 2. Division of Neurology, Department of Pediatrics; University of Toronto, Hospital for Sick Children; Toronto Ontario
  • 3. Division of Neurology; University of Alberta; Edmonton Alberta
  • 4. Division of Neurology, University Hospital Center of Quebec and Faculty of Medicine; Laval University; Quebec City Quebec Canada

Description

This is the peer reviewed version of the following article: [Gan-Or, Z., Yoon, G., Suchowersky, O., Dupré, N., and Rouleau, G.A. (2017). KCNA2 mutations are rare in hereditary spastic paraplegia. Annals of Neurology 81, 325–326.], which has been published in final form at https://doi.org/10.1002/ana.24855. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.

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