Hereditary hyperferritinemia cataract syndrome: a de novo mutation in the iron responsive element of the L-ferritin gene

Haematologica. 1999 Jun;84(6):560-1.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Cataract / blood*
  • Cataract / genetics*
  • Family Health
  • Ferritins / blood*
  • Ferritins / genetics*
  • Humans
  • Iron / metabolism*
  • Iron Metabolism Disorders / genetics*
  • Male
  • Pedigree
  • Point Mutation
  • Syndrome

Substances

  • Ferritins
  • Iron