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The Wiskott-Aldrich Syndrome: The Actin Cytoskeleton and Immune Cell Function
Wiskott-Aldrich syndrome (WAS) is a rare X-linked recessive primary immunodeficiency characterised by immune dysregulation, microthrombocytopaenia, eczema and lymphoid malignancies. Mutations in the WAS gene can lead to distinct syndrome variations which largely, although not exclusively, depend upo...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
IOS Press
2010
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3835520/ https://ncbi.nlm.nih.gov/pubmed/21178275 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/DMA-2010-0735 |
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