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

Academic Press

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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)

By Luthi J.N.   Gandhi M.J.   Drachman J.G.  

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

Elsevier

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A Novel Protocol to Identify Mutations in Patients with Wiskott–Aldrich Syndrome

By Jones L.N.   Lutskiy M.I.   Cooley J.   Kenney D.M.   Rosen F.S.   Remold-O'Donnell E.  

Blood Cells, Molecules, and Diseases, Vol. 28, Iss. 3, 2002-03 ,pp. : 392-398

Academic Press

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Absence of Expression of the Wiskott–Aldrich Syndrome Protein in Peripheral Blood Cells of Wiskott–Aldrich Syndrome Patients

By MacCarthy-Morrogh L.   Gaspar H.B.   Wang Y-C.   Katz F.   Thompson L.   Layton M.   Jones A.M.   Kinnon C.  

Clinical Immunology, Vol. 88, Iss. 1, 1998-07 ,pp. : 22-27

Academic Press

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The Wiskott-Aldrich syndrome

By Ochs Hans  

Clinical Reviews in Allergy and Immunology, Vol. 20, Iss. 1, 2001-02 ,pp. : 61-86

Humana Press, Inc

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