POLR3A variants in hereditary spastic paraplegia and ataxia

Brain. 2018 Jan 1;141(1):e1. doi: 10.1093/brain/awx290.
No abstract available

Publication types

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

MeSH terms

  • Humans
  • Intellectual Disability
  • Muscle Spasticity
  • Mutation
  • Optic Atrophy*
  • RNA Polymerase III / genetics
  • Spastic Paraplegia, Hereditary / genetics*
  • Spinocerebellar Ataxias / genetics*

Substances

  • POLR3A protein, human
  • RNA Polymerase III

Supplementary concepts

  • Spastic Ataxia