Associated Papers
Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome.
O'Connell AE et al.
Frontiers in Immunology, 2014
The c.273+11dup genetic change in the WAS gene is a functionally neutral polymorphism.
Jeanson-Leh L et al.
European Journal of Haematology, 2011
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
Proust A et al.
Blood Cells, Molecules & Diseases, 0
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