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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...

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Bibliografische gegevens
Hoofdauteurs: Blundell, Michael P., Worth, Austen, Bouma, Gerben, Thrasher, Adrian J.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: IOS Press 2010
Onderwerpen:
Online toegang: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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