A Case of HSP Carrying c.1537-11A > G Mutation of the SPAST Gene Presented as Stiff-Person Syndrome

Neurol India. 2021 Jul-Aug;69(4):1053-1054. doi: 10.4103/0028-3886.325344.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Humans
  • Mutation
  • Spastic Paraplegia, Hereditary*
  • Spastin / genetics
  • Stiff-Person Syndrome* / genetics

Substances

  • Spastin
  • SPAST protein, human