Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in SLC39A14 Mutation Carriers and Genetic Animal Models Review

Rodichkin, Alexander N, Guilarte, Tomas R. (2022). Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in SLC39A14 Mutation Carriers and Genetic Animal Models . International Journal of Molecular Sciences, 23(21), 10.3390/ijms232112833

Open Access

cited authors

  • Rodichkin, Alexander N; Guilarte, Tomas R

sustainable development goals

authors

publication date

  • November 1, 2022

published in

keywords

  • ACCUMULATION
  • BRAIN
  • Biochemistry & Molecular Biology
  • Chemistry
  • Chemistry, Multidisciplinary
  • HISTORY
  • HYPERMANGANESEMIA
  • Life Sciences & Biomedicine
  • MICE
  • MOTOR DEFICITS
  • POLYCYTHEMIA
  • Physical Sciences
  • SLC30A10 MUTATIONS
  • Science & Technology
  • Slc39a14
  • TRANSPORTER
  • dystonia-parkinsonism
  • manganese
  • manganism

Digital Object Identifier (DOI)

volume

  • 23

issue

  • 21