Neuroferritinopathy in a French family with late onset dominant dystonia

J Med Genet. 2003 May;40(5):e69. doi: 10.1136/jmg.40.5.e69.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Basal Ganglia Diseases / genetics*
  • Basal Ganglia Diseases / pathology*
  • Basal Ganglia Diseases / physiopathology
  • Corpus Striatum / pathology
  • Dystonia / genetics*
  • Dystonia / pathology*
  • Dystonia / physiopathology
  • England
  • France
  • Genes, Dominant / genetics*
  • Haplotypes / genetics
  • Humans
  • Iron / metabolism*
  • Middle Aged

Substances

  • Iron