Article
The Wiskott-Aldrich Syndrome: The Actin Cytoskeleton and Immune Cell Function
2010-01-01
Abstract excerpt
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 upon the mutation. Premature termination and deletions abrogate Wiskott-Aldrich syndrome protein (WASp) expression and l...
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Identifiers and source
- Literature Corpus work
- 4d3a3a30-6e61-5e21-b3ce-7dacc5a2dbc9
- DOI
- 10.1155/2010/781523
