GLUT1 deficiency and pediatric-onset hereditary spastic paraplegia: A new association

Alberto Verrotti, Ludovica Di Francesco, Pasquale Striano

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)233-234
Number of pages2
JournalEuropean Journal of Paediatric Neurology
Volume23
Issue number2
DOIs
Publication statusPublished - Mar 2019

Keywords

  • Child
  • Glucose Transporter Type 1
  • Humans
  • Mutation
  • Spastic Paraplegia, Hereditary

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