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  • Molecular assay reagents intended to identify deletions or duplications of the Wiskott-Aldrich syndrome (WAS) gene, located at chromosome Xp11.23, which encodes the Wiskott-Aldrich syndrome protein. Genetic variants at this locus have been associated with Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, and X-linked thrombocytopenia.
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