Article thumbnail

A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia

By Marina Diomedi, Ziv Gan-Or, Fabio Placidi, Patrick A. Dion, Anna Szuto, Mario Bengala, Guy A. Rouleau and Gian Luigi Gigli
Publisher: Elsevier BV
Year: 2016
DOI identifier: 10.1016/j.ejmg.2016.10.003
OAI identifier:
Provided by: MUCC (Crossref)
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • (external link)
  • Suggested articles

    To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.