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A boy with X-linked hyper-IgM syndrome and natural killer cell deficiency

We present a boy with hyper-IgM syndrome with a previously not reported mutation in the CD40 ligand gene. He also had a concomitant natural killer (NK) cell deficiency. He had no CD56(+) or CD16(+) cells and no NK activity as determined in 4 h chromium release cytotoxicity assay. After 5 days in cul...

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Détails bibliographiques
Auteurs principaux: ØSTENSTAD, B, GILIANI, S, MELLBYE, O J, NILSEN, B R, ABRAHAMSEN, T
Format: Artigo
Langue:Inglês
Publié: Blackwell Science Inc 1997
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1904570/
https://ncbi.nlm.nih.gov/pubmed/9030857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2249.1997.284-ce1174.x
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