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A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP
A female offspring of consanguineous parents, showed features of Wiskott-Aldrich syndrome (WAS), including recurrent infections, eczema, thrombocytopenia, defective T cell proliferation and chemotaxis, and impaired natural killer cell function. Cells from this patient had undetectable WAS protein (W...
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| Huvudupphovsmän: | , , , , , , , , , , , , , , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
The Rockefeller University Press
2012
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3260865/ https://ncbi.nlm.nih.gov/pubmed/22231303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1084/jem.20110896 |
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