Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion

Mov Disord. 2019 Dec;34(12):1931-1932. doi: 10.1002/mds.27905.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • ATPases Associated with Diverse Cellular Activities
  • DNA, Mitochondrial
  • Humans
  • Metalloendopeptidases
  • Paraplegia
  • Parkinsonian Disorders*
  • Spastic Paraplegia, Hereditary*

Substances

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

Supplementary concepts

  • Spastic Paraplegia Type 7