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Article

Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients.

Iranian journal of allergy, asthma, and immunology - 1 Dec 2012

Safaei Sepideh, Fazlollahi Mohammad Reza, Houshmand Masoud, Hamidieh Amir Ali, Bemanian Mohammad Hassan, Alavi Samin, Mousavi Farideh, Pourpak Zahra, Moin Mostafa

Abstract excerpt

Wiskott-Aldrich syndrome (WAS) is a life-threatening X-linked recessive immunodeficiency disease described as a clinical triad of thrombocytopenia, eczema, and recurrent infections, caused by mutations of the WAS protein (WASP) gene. The milder form of this disease is X-linked thrombocytopenia (XLT) that presents only as platelet abnormalities. Mutation analysis for 15 boys with Wiskott-Aldrich syndrome was...

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PMID: 23264413
DOI: 011.04/ijaai.345348

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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