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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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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
1997
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| Assuntos: | |
| Acesso em linha: | 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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