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Article

The genotype of the original Wiskott phenotype.

The New England journal of medicine - 26 Oct 2006

Binder Vera, Albert Michael H, Kabus Maria, Bertone Marko, Meindl Alfons, Belohradsky Bernd H

Abstract excerpt

The Wiskott-Aldrich syndrome is an X-linked hereditary disorder associated with combined immunodeficiency, thrombocytopenia, small platelets, eczema, and increased susceptibility to autoimmune disorders and cancers. It is caused by mutations in the gene (WAS) for the Wiskott-Aldrich syndrome prot...

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Identifiers

PMID: 17065640
DOI: 10.1056/NEJMoa062520

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17065640-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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