Molecular and haematological studies of four families with hereditary spherocytosis resulting from band 3 deficiency

Acta Haematol. 2006;116(2):143-5. doi: 10.1159/000093647.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Amino Acid Substitution
  • Anion Exchange Protein 1, Erythrocyte / deficiency*
  • Base Sequence
  • Child
  • Female
  • Humans
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Mutation, Missense
  • Nucleic Acid Conformation
  • Spherocytosis, Hereditary / etiology
  • Spherocytosis, Hereditary / genetics*

Substances

  • Anion Exchange Protein 1, Erythrocyte