X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP)

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Experimental Hematology, Vol. 31, Iss. 2, 2003-02 ,pp. : 150-158

Elsevier

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Clinical Aspects and Genetic Analysis of Taiwanese Patients with Wiskott–Aldrich Syndrome Protein Mutation: The First Identification of X-Linked Thrombocytopenia in the Chinese with Novel Mutations

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Journal of Clinical Immunology, Vol. 30, Iss. 4, 2010-07 ,pp. : 593-601

Springer Publishing Company

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Unique and Recurrent WAS Gene Mutations in Wiskott-Aldrich Syndrome and X-Linked Thrombocytopenia

By Thompson L.J.   Lalloz M.R.A.   Weatherall D.S.D.M.  

Blood Cells, Molecules, and Diseases, Vol. 25, Iss. 4, 1999-08 ,pp. : 218-226

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Distinct Interactions of the X-Linked Lymphoproliferative Syndrome Gene Product SAP with Cytoplasmic Domains of Members of the CD2 Receptor Family

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X-linked hyper IgM syndrome

By Schneider Lynda  

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