Molecular basis for the hereditary hyperferritinemia-cataract syndrome

Blood. 1996 Jun 1;87(11):4912-3.
No abstract available

Publication types

  • Letter

MeSH terms

  • Base Sequence
  • Cataract / genetics*
  • Cataract / metabolism
  • Chromosomes, Human, Pair 19
  • Ferritins / blood*
  • Humans
  • Iron / physiology
  • Models, Biological
  • Molecular Sequence Data
  • Phenotype
  • Point Mutation
  • Regulatory Sequences, Nucleic Acid
  • Syndrome

Substances

  • Ferritins
  • Iron