High frequency of C4 "null" alleles in primary antiphospholipid syndrome

Ann Med Interne (Paris). 1996;147(2):115-6.
No abstract available

MeSH terms

  • Adult
  • Antiphospholipid Syndrome / genetics*
  • Complement C4 / genetics*
  • Disease Susceptibility
  • Female
  • Humans
  • Male
  • Middle Aged
  • Phenotype

Substances

  • Complement C4