Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon-Reference-Cited by-同舟云学术

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Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon

Published:2020-10 Issue: Volume:219 Page:108573
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Mansour Rana,El-Orfali Youmna,Saber Antoine,Noun Dolly,Youssef Nour,Youssef Yolla,Hanna-Wakim Rima,Dbaibo Ghassan,Abboud Miguel,Massaad Michel J.

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference74 articles.

1. Wiskott-Aldrich syndrome: a comprehensive review;Massaad;Ann. N. Y. Acad. Sci.,2013

2. Disease mechanism: unravelling Wiskott-Aldrich syndrome;Kirchhausen;Curr. Biol.,1996

3. A multiinstitutional survey of the Wiskott-Aldrich syndrome;Sullivan;J. Pediatr.,1994

4. X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene;Villa;Nat. Genet.,1995

5. The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene;Zhu;Blood,1995

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Novel Splicing Mutation Leading to Wiskott-Aldrich Syndrome from a Family;International Journal of Genomics;2024-02-19

2. The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity;Journal of Allergy and Clinical Immunology;2023-12

3. A novel homozygous mutation in RASGRP1 that predisposes to immune dysregulation and immunodeficiency associated with uncontrolled Epstein-Barr virus-induced B cell proliferation;Clinical Immunology;2023-12

4. Sinonasal diffuse large B-cell lymphoma in a patient with Wiskott–Aldrich syndrome: A case report and literature review;Frontiers in Immunology;2023-01-12

5. Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variants;The American Journal of Human Genetics;2021-12

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