Human properdin deficiency has a heterogeneous genetic background

Immunopharmacology. 1997 Dec;38(1-2):203-6. doi: 10.1016/s0162-3109(97)00087-8.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Genetic Linkage
  • Humans
  • Male
  • Meningococcal Infections / genetics*
  • Meningococcal Infections / immunology
  • Mutation / genetics*
  • Phenotype
  • Properdin / deficiency*
  • Properdin / genetics*
  • Properdin / immunology
  • X Chromosome / genetics

Substances

  • Properdin