Broadening the clinical spectrum of FUS mutations: a case with monomelic amyotrophy with a late progression to amyotrophic lateral sclerosis

Neurol Sci. 2021 Mar;42(3):1207-1209. doi: 10.1007/s10072-020-04751-5. Epub 2020 Oct 1.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis* / complications
  • Amyotrophic Lateral Sclerosis* / genetics
  • Humans
  • Mutation
  • RNA-Binding Protein FUS* / genetics
  • Spinal Muscular Atrophies of Childhood*

Substances

  • FUS protein, human
  • RNA-Binding Protein FUS

Supplementary concepts

  • Amyotrophy, monomelic