Localization of the genetic defect in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1) to the CD40 ligand gene

Trans Assoc Am Physicians. 1993:106:91-5.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Antigens, CD / metabolism
  • Antigens, Differentiation, B-Lymphocyte / metabolism
  • CD40 Antigens
  • CD40 Ligand
  • Child
  • Child, Preschool
  • DNA Mutational Analysis
  • Dysgammaglobulinemia / complications
  • Dysgammaglobulinemia / genetics*
  • Dysgammaglobulinemia / immunology
  • Gene Expression
  • Genetic Linkage
  • Humans
  • Hypergammaglobulinemia / complications
  • Hypergammaglobulinemia / genetics*
  • Hypergammaglobulinemia / immunology
  • IgA Deficiency / complications
  • IgA Deficiency / genetics
  • IgA Deficiency / immunology
  • IgG Deficiency / complications
  • IgG Deficiency / genetics
  • IgG Deficiency / immunology
  • Immunoglobulin M / blood*
  • In Vitro Techniques
  • Male
  • Membrane Glycoproteins / genetics*
  • Membrane Glycoproteins / metabolism
  • Pedigree
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • T-Lymphocytes / immunology
  • X Chromosome*

Substances

  • Antigens, CD
  • Antigens, Differentiation, B-Lymphocyte
  • CD40 Antigens
  • Immunoglobulin M
  • Membrane Glycoproteins
  • RNA, Messenger
  • CD40 Ligand