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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
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Provided by: MUCC (Crossref)
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