Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria

N Engl J Med. 1990 Oct 25;323(17):1184-9. doi: 10.1056/NEJM199010253231707.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Acetylcholinesterase / analysis
  • Adult
  • Blood Proteins / analysis
  • Blood Proteins / deficiency*
  • CD55 Antigens
  • CD59 Antigens*
  • Carrier Proteins* / analysis
  • Cell Separation
  • Cells, Cultured
  • Erythrocyte Membrane* / chemistry
  • Fibroblasts / chemistry
  • Flow Cytometry
  • Hemoglobinuria, Paroxysmal / blood
  • Hemoglobinuria, Paroxysmal / genetics*
  • Humans
  • Immunohistochemistry
  • Male
  • Membrane Proteins / analysis

Substances

  • Blood Proteins
  • CD55 Antigens
  • CD59 Antigens
  • Carrier Proteins
  • Membrane Proteins
  • CD59 protein, human
  • Acetylcholinesterase