KCNA2 mutations are rare in hereditary spastic paraplegia

Ann Neurol. 2017 Feb;81(2):325-326. doi: 10.1002/ana.24855.
No abstract available

Publication types

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

MeSH terms

  • Ataxia
  • Databases, Genetic
  • Humans
  • Kv1.2 Potassium Channel
  • Mutation
  • Spastic Paraplegia, Hereditary*

Substances

  • KCNA2 protein, human
  • Kv1.2 Potassium Channel

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