Hereditary hyperferritinemia-cataract syndrome: two novel mutations in the L-ferritin iron-responsive element

Blood. 1998 Jan 1;91(1):367-8.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Adult
  • Age of Onset
  • Apoferritins
  • Base Sequence
  • Cataract / epidemiology
  • Cataract / genetics*
  • Female
  • Ferritins / blood*
  • Ferritins / genetics*
  • Gene Expression Regulation
  • Humans
  • Iron*
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Nucleic Acid Conformation
  • Point Mutation*
  • Regulatory Sequences, Nucleic Acid*
  • Syndrome

Substances

  • Ferritins
  • Apoferritins
  • Iron