X-linked hyper IgM

R. L. Fuleihan*, R. S. Geha

*Corresponding author for this work

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

X-linked hyper IgM (X-HIM) is a rare inherited immune deficiency that has recently been shown to result from a defect in the gene for CD40 ligand (CD40L). Here, Ramsay L. Fuleihan and Raif S. Geha describe the clinical and pathological features of this disease, its pathogenesis, and current as well as potential future therapies.

Original languageEnglish (US)
Pages (from-to)133-136
Number of pages4
JournalImmunologist
Volume5
Issue number4
Publication statusPublished - Jan 1 1997

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ASJC Scopus subject areas

  • Immunology
  • Cell Biology

Cite this

Fuleihan, R. L., & Geha, R. S. (1997). X-linked hyper IgM. Immunologist, 5(4), 133-136.