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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Detalles Bibliográficos
Autores principales: Blundell, Michael P., Worth, Austen, Bouma, Gerben, Thrasher, Adrian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2010
Materias:
Other
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835520/
https://www.ncbi.nlm.nih.gov/pubmed/21178275
http://dx.doi.org/10.3233/DMA-2010-0735

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835520/
https://www.ncbi.nlm.nih.gov/pubmed/21178275
http://dx.doi.org/10.3233/DMA-2010-0735

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