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  • Molecular assay reagents intended to identify mutations in the Wiskott-Aldrich syndrome (WAS) gene, located at chromosome Xp11.4-p11.21, which encodes for one of a family of proteins involved in the transduction of signals from receptors on cell surfaces to the actin cytoskeleton. This X-linked inherited genetic mutation has been identified in patients with WAS-related disorders, a spectrum of early (infant) onset disorders of the hematopoietic cells in males.
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