Novel homozygous SPG7 missense mutation in a Chinese hereditary spastic paraplegia family

Acta Neurol Belg. 2020 Dec;120(6):1453-1455. doi: 10.1007/s13760-020-01286-6. Epub 2020 Jan 30.
No abstract available

Publication types

  • Letter

MeSH terms

  • ATPases Associated with Diverse Cellular Activities / genetics*
  • Asian People / genetics
  • Female
  • Humans
  • Male
  • Metalloendopeptidases / genetics*
  • Mutation, Missense
  • Pedigree
  • Spastic Paraplegia, Hereditary / genetics*
  • Young Adult

Substances

  • Metalloendopeptidases
  • SPG7 protein, human
  • ATPases Associated with Diverse Cellular Activities