Molecular characterization of two Malaysian patients with Wiskott-Aldrich syndrome

The Wiskott-Aldrich Syndrome (WAS) is an X-linked immunodeficiency condition characterized by microthrombocytopenia, eczema and recurrent infections. It is caused by mutations in the Wiskott-Aldrich Syndrome protein (WASP) gene. We investigated two Malay boys who presented with congenital thrombocyt...

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Bibliographic Details
Main Author: Farah Nadhirah
Other Authors: Mohd Farid Baharin
Format: Journal
Published: Malaysian Journal of Pathology, Academy of Medicine of Malaysia 2015
Subjects:
Online Access:http://www.myjurnal.my/public/article-view.php?id=90280