Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiencyTNFRSF13B/TACI deficiency
The presence of a second TNFRSF13B mutation, HLA class II markers, or multiple single nucleotide variants in patients helps to explain the incomplete penetrance of immunodeficiency in carriers of TNFRSF13B mutations.
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| Hlavní autoři: | , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Rockefeller University Press
2025-08-01
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| Edice: | Journal of Human Immunity |
| On-line přístup: | https://rupress.org/jhi/article-pdf/doi/10.70962/jhi.20250016/1949050/jhi_20250016.pdf |
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