The Wiskott–Aldrich syndrome: from genotype–phenotype correlation to treatment
Author:
Publisher
Informa UK Limited
Subject
Immunology,Immunology and Allergy
Link
http://www.tandfonline.com/doi/pdf/10.1586/1744666X.3.5.813
Reference72 articles.
1. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
2. X–linked thrombocytopenia and Wiskott–Aldrich syndrome are allelic diseases with mutations in the WASP gene
3. Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia
4. Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia
5. Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia
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2. Understanding immunoactinopathies: A decade of research on WAS gene defects;Pediatric Allergy and Immunology;2023-04
3. СИНДРОМ ВИСКОТТА-ОЛДРИЧА. КРАТКОЕ ОПИСАНИЕ БОЛЕЗНИ;Международный журнал научной педиатрии;2022-11-30
4. Atopic Dermatitis-like Genodermatosis: Disease Diagnosis and Management;Diagnostics;2022-09-09
5. Clinical Features, Cancer Biology, Transplant Approach and Other Integrated Management Strategies for Wiskott–Aldrich Syndrome;Journal of Multidisciplinary Healthcare;2021-12
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