DCTN1 mutation associated parkinsonism: case series of three new families with perry syndrome

J Neurol. 2022 Dec;269(12):6667-6672. doi: 10.1007/s00415-022-11308-3. Epub 2022 Jul 27.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Depression
  • Dynactin Complex / genetics
  • Humans
  • Hypoventilation* / genetics
  • Mutation / genetics
  • Parkinsonian Disorders* / diagnostic imaging
  • Parkinsonian Disorders* / genetics

Substances

  • Dynactin Complex
  • DCTN1 protein, human

Supplementary concepts

  • Perry Syndrome