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

Eur J Paediatr Neurol. 2019 Mar;23(2):233-234. doi: 10.1016/j.ejpn.2019.02.010.
No abstract available

Publication types

  • Editorial
  • Comment

MeSH terms

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

Substances

  • Glucose Transporter Type 1
  • SLC2A1 protein, human