Identification of a novel WAS mutation in a South African patient presenting with atypical Wiskott-Aldrich syndrome: a case report
Abstract Background The X-linked recessive primary immunodeficiency disease (PIDD) Wiskott-Aldrich syndrome (WAS) is identified by an extreme susceptibility to infections, eczema and thrombocytopenia with microplatelets. The syndrome, the result of mutations in the WAS gene which encodes the Wiskott...
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| Main Authors: | , , , , , , , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2020-06-01T00:00:00Z.
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