Atypical clinical presentation and typical FTD atrophy: 17-year clinical follow-up and MRI analysis of a slowly progressive bvFTD associated with C9orf72 expansion

Rev Neurol (Paris). 2020 Sep;176(7-8):627-629. doi: 10.1016/j.neurol.2020.02.003. Epub 2020 Mar 13.
No abstract available

Publication types

  • Letter

MeSH terms

  • Amyotrophic Lateral Sclerosis* / genetics
  • Atrophy
  • C9orf72 Protein / genetics
  • DNA Repeat Expansion
  • Follow-Up Studies
  • Frontotemporal Dementia* / genetics
  • Humans
  • Magnetic Resonance Imaging

Substances

  • C9orf72 Protein
  • C9orf72 protein, human