Delineating the phenotype of autosomal-recessive HPCA mutations: Not only isolated dystonia!

Mov Disord. 2019 Apr;34(4):589-592. doi: 10.1002/mds.27638.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Dystonia / genetics*
  • Dystonic Disorders / genetics*
  • Hippocalcin / genetics
  • Humans
  • Mutation
  • Phenotype

Substances

  • HPCA protein, human
  • Hippocalcin