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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Detaylı Bibliyografya
Asıl Yazarlar: Blundell, Michael P., Worth, Austen, Bouma, Gerben, Thrasher, Adrian J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: IOS Press 2010
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Other
Online Erişim: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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